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Nevoid basal-cell carcinoma syndrome - Wikipedi

Gorlin syndrome, also known as nevoid basal cell carcinoma syndrome, is a condition that affects many areas of the body and increases the risk of developing various cancerous and noncancerous tumors. In people with Gorlin syndrome, the type of cancer diagnosed most often is basal cell carcinoma, which is the most common form of skin cancer From Wikipedia, the free encyclopedia Goldenhar syndrome is a rare congenital defect characterized by incomplete development of the ear, nose, soft palate, lip and mandible on usually one side of the body. Common clinical manifestations include limbal dermoids, preauricular skin tags and strabismus Gorlin sendromu (Gorlin syndrome), vücudun birçok alanını etkileyen ve çeşitli kanserli ve kanserli olmayan tümörleri geliştirme riskini artıran otozomal dominant kalıtsal bir hastalıktır.. Genellikle cildi, endokrin sistemi, sinir sistemini, gözleri ve kemikleri etkiler. Gorlin sendromu ayrıca Gorlin-Goltz sendromu, bazal hücreli nevus sendromu ve nevoid bazal hücreli. The name Gor­lin syndrome refers to the Amer­i­can oral pathol­o­gist and human ge­neti­cist Robert J. Gor­lin (1923-2006). The Amer­i­can der­ma­tol­o­gist Robert W. Goltz (1923-2014) was his co-au­thor, which is the basis for the term 'Gor­lin-Goltz syn­drome'

Nevoid basal cell carcinoma syndrome - Libre Patholog

  1. Gorlin syndrome is a rare condition in which many people develop a type of skin cancer called basal cell cancer of the skin. They might also have a number of other medical conditions. How common is it Gorlin syndrome affects about 1 in 31,000 people, although the true figure may be higher as mild cases can go unrecognised
  2. 1 Instructions for Filling in this Page 2 Summary 3 Symptom Description 4 Photo Evidence 5 Video Evidence 6 Diagnosis and Detection 7 Scientific Findings Summary 7.1 Puzzle Pieces I: Associated Chromosomes and Genes 7.2 Puzzle Pieces II: Chromosome and Gene Regular Functionement 7.3 Puzzle Pieces III: Chromosome and Gene Disfunction 7.4 Puzzle Pieces IV: Evolution 8 Sources: Bibliography and.
  3. Goldenhar syndrome (GS) is characterized by craniofacial anomalies in association with vertebral, cardiac, renal, and central nervous system defects. The syndrome is characterized by a triad of anomalies comprising epibulbar dermoid, accessory auricular appendages, and aural fistula

Gorlin-Chaudhry-Moss syndrome is an extremely rare inherited disorder characterized by premature closure of the fibrous joints (sutures) between certain bones in the skull (craniosynostosis), unusually small eyes (microphthalmia), absence of some teeth (hypodontia), and/or excessive amounts of hair (hypertrichosis) on most areas of the body Collapse Section Meier-Gorlin syndrome is a condition primarily characterized by short stature. It is considered a form of primordial dwarfism because the growth problems begin before birth (intrauterine growth retardation). After birth, affected individuals continue to grow at a slow rate

Gorlin - Wikipedi

  1. ant fashion with complete penetrance and variable expressivity
  2. The clinical findings of Goltz syndrome can overlap with those of other ectodermal dysplasia syndromes and are variable in presentation. This complicates diagnosis and further characterization of these disorders. Goltz syndrome is a rare genetic condition characterized by involvement of the skin, skeletal system, eyes, and face
  3. Consequently, the disorder is also known as Gorlin syndrome or Gorlin-Goltz syndrome. Over the years, case reports and series have continued to expand the range of symptoms and physical findings that can be associated with NBCCS, and there are now more than 100 different recognized features

Gorlin syndrome - a syndrome of myriad basal cell nevi with development of basal cell carcinomas in adult life. Synonym (s): basal cell nevus syndrome Gorlin-Chaudhry-Moss syndrome - craniofacial dysostosis, patent ductus arteriosus, hypertrichosis, hypoplasia of the labia majora, and dental and ocular abnormalities. Medical Eponyms © Farlex 201 The focal dermal hypoplasia , also known as Goltz-Gorlin syndrome , is a rare genetic disease from the group of phacomatoses . The Gorlin-Goltz syndrome or basal cell nevus syndrome must be distinguished from this, which is much more common and in which basaliomas occur more frequently The Gorlin-Chaudhry-Moss Syndrome (GCM) is a very rare congenital disease with a combination of craniofacial malformation, hearing loss, general hypertrichosis and other malformations.. Synonyms are: GCM syndrome; Craniofacial dysostosis with genital, dental and cardiac abnormalities; Craniofacial dysostosis-hypertrichosis-hypoplasia of the labia majora syndrome; English Fontaine progeroid.

Gorlin-Goltz syndrome. Dr Bahman Rasuli and Dr Gagandeep Singh et al. Gorlin-Goltz syndrome (also known as the basal cell nevus syndrome, nevoid basal cell carcinoma syndrome, or just Gorlin syndrome) is a rare phakomatosis characterized by multiple odontogenic keratocysts (OKC) , multiple basal cell carcinomas (BCC) and other abnormalities. On. Synonyms for basal cell naevus syndrome (BCNS) include basal cell carcinoma nevus syndrome (BCCNS), Gorlin-Goltz syndrome, Gorlin syndrome, and nevoid basal cell carcinoma syndrome. The so-called basal cell naevi are actually tiny basal cell carcinomas. Developmental abnormalities in affected individuals may include: Odontogenic cysts in the ja Focal dermal hypoplasia is a genetic disorder that primarily affects the skin, skeleton, eyes, and face. The skin abnormalities are present from birth and can include streaks of very thin skin (dermal hypoplasia), cutis aplasia, and telangiectases.They also may abnormalities in the nails, hands, and feet nevoid basal cell carcinoma syndrome: [nē′void] an inherited form of premalignant skin lesion. It is an autosomal-dominant trait, but the cause is unknown. It is associated with other abnormalities of the skin or bone, the nervous system, the eyes, and the reproductive system. It affects persons under the age of 20 and is accompanied by palmar.

plural of Gorlin's syndrome Definition from Wiktionary, the free dictionar Gorlin's syndrome. Definition from Wiktionary, the free dictionary. Jump to navigation Jump to search. English Etymology . For Robert J. Gorlin, US physician. Noun . Gorlin's syndrome (plural Gorlin's syndromes) Either of nevoid basal cell carcinoma syndrome and focal dermal hypoplasia. Retrieved. Gorlin sendromu (Basal cell nevi; Nevoid basal cell carcinoma; Gorlin-Goltz sendromu), otosomal dominant yolla aktarılan, deride tümörler ve kistler, çene kemiklerinde odontojen keratokistik tümörler, dudak ve damak yarığı, beyin zarında kireçlenmeler, avuçlarda ve tabanlarda çukurcuklar, çeşitli tümörler, mezanter kistleri ve kemik malformasyonları içeren kalıtsal bir. La sindrome di Gorlin, nota anche come sindrome del carcinoma basocellulare nevoide (NBCCS) scoperta per la prima volta nel 1960, è un raro disordine ereditario a trasmissione autosomica dominante ad alta penetranza e variabile espressività, che si manifesta con anomalie di sviluppo e predisposizione a sviluppare vari tipi di neoplasie (tumori) probabilmente per alterazione della normale via. In medicine, the Gorlin sign is the ability to touch the tip of the nose with the tongue. Approximately ten percent of the general population can perform this act, whereas fifty percent of people with the inherited connective tissue disorder, Ehlers-Danlos syndrome, can. Named after pathologist Robert J. Gorlin, it should not be confused with Gorlin syndrome, a more serious condition also.

Gorlin's sign. Gorlin sign is the ability to touch the tip of the nose with the tongue. Approximately ten percent of the general population can perform this act, whereas five times as many people with Ehlers-Danlos syndrome can. It is not to be confused with Gorlin syndrome Angel A. Alvarez, Markus Bredel, in Emery and Rimoin's Principles and Practice of Medical Genetics, 2013 124.4.6 Gorlin Syndrome. Gorlin syndrome, also called nevoid basal cell carcinoma syndrome, is an autosomal dominant disorder leading to the development of multiple basal cell carcinomas of the skin as well as palmar and plantar pits, odontogenic keratocysts, and skeletal anomalies (30)

Gorlin syndrome. Gorlin syndrome, also known as nevoid basal cell carcinoma syndrome, is a condition that affects many areas of the body and increases the risk of developing various cancerous and noncancerous tumors.. In people with Gorlin syndrome, the type of cancer diagnosed most often is basal cell carcinoma, which is the most common form of skin cancer Gorlin Syndrome is caused by a mutation of genes involved the the Sonic Hedgehog Signalling Pathway. It is a dominant characteristic, therefore you see effects of such a mutation in single dose; where there is one chromosome carrying a relevant mutated gene, while the other chromosome of that pair carries a normal copy of the same gene

Gorlin-Goltz Syndrome - zxc

Gorlin syndrome or Nevoid Basal Cell Carcinoma syndrome is a medical condition affecting many body systems and is caused by a fault in just one of the thousands of genes which humans possess. The condition is characterised by the development of multiple jaw cysts (keratocysts) frequently beginning in the second decade of life and/or basal cell. PTCH, the human homologue of the Drosophila segment polarity gene, patched, has been identified as the gene responsible for Gorlin or nevoid basal cell carcinoma syndrome (NBCCS). We report here the characterization of four novel mutations in the human PTCH gene in germ-line DNA from Gorlin patients Although a variety of eponyms have been proposed for MEN2B (e.g. Williams-Pollock syndrome, Gorlin-Vickers syndrome, and Wagenmann-Froboese syndrome), none ever gained sufficient traction to merit continued use and, indeed, are all but abandoned in the medical literature. Another early report was Schimke et al in 1968 Gorlin was born in Hudson, New York. After receiving an A.B. degree in 1943 from Columbia University, Gorlin volunteered for the Army, where he was instructed to apply to dental school.He graduated in 1947 from Washington University Dental School in St. Louis, Missouri, and then completed a master's degree in oral pathology from the State University of Iowa (now the University of Iowa), Iowa. The name Gorlin syndrome refers to the American oral pathologist and human geneticist Robert J. Gorlin (1923-2006). Nevoid basal-cell carcinoma syndrome_sentence_3 The American dermatologist Robert W. Goltz (1923-2014) was his co-author, which is the basis for the term 'Gorlin-Goltz syndrome'

Focal dermal hypoplasia - Wikipedi

Turcot syndrome is a condition characterized by multiple adenomatous colon polyps, an increased risk of colorectal cancer, and an increased risk of brain cancer. It may be associated with familial adenomatous polyposis (FAP) or Lynch syndrome (also known as hereditary non-polyposis colorectal cancer or HNPCC). The molecular basis of most Turcot. The nevoid BCC syndrome or Gorlin's syndrome is a condition with significant oral, head and neck involvement that occurs at a younger age (under 30 years) and should be recognized by dentists. It has been explored that medullated nerve fibres are a sign of Gorlin's syndrome - a feature of which is intracranial calcification Robert James Gorlin synonyms, Robert James Gorlin pronunciation, Robert James Gorlin translation, English dictionary definition of Robert James Gorlin. n 1. a rare congenital disorder in which cancer destroys the facial skin and causes blindness; skeletal anomalies and some mental retardation can also occur..

The name Gorlin syndrome refers to the American oral pathologist and human geneticist Robert J. Gorlin (1923-2006). The American dermatologist Robert W. Goltz (1923-2014) was his co-author, which is the basis for the term 'Gorlin-Goltz syndrome'. First described in 1960 by Gorlin and Goltz, NBCCS is an autosomal dominant condition that can. Synonyms for Gorlin Syndrome in Free Thesaurus. Antonyms for Gorlin Syndrome. 7 synonyms for syndrome: condition, complaint, illness, symptoms, disorder, ailment, affliction. What are synonyms for Gorlin Syndrome

Vingt-et-un pour cent des patients étaient atteints d'un syndrome de Gorlin.: Twenty-one percent of patients carried a diagnosis of Gorlin syndrome.: Il existe une hétérogénéité génétique dans le syndrome de Gorlin avec quelques familles rapportées avec des mutations dans les gènes SUFU et PTCH2.: Gorlin syndrome displays genetic heterogeneity, with some families reported with SUFU. Gorlin syndrome synonyms, Gorlin syndrome pronunciation, Gorlin syndrome translation, English dictionary definition of Gorlin syndrome. n 1. a rare congenital disorder in which cancer destroys the facial skin and causes blindness; skeletal anomalies and some mental retardation can also occur.. Welcome to the NicknameDB entry on gorlin syndrome nicknames! Below you'll find name ideas for gorlin syndrome with different categories depending on your needs. According to Wikipedia: Nevoid basal-cell carcinoma syndrome (NBCCS), is an inherited medical condition involving defects within multiple body systems such as the skin, nervous system, eyes, endocrine system, and bones Gorlin-Goltz syndrome, also known as the basal cell naevus syndrome, is a rare phakomatosis characterised by multiple odontogenic keratocysts (KOT), multiple . Gorlin and Goltz's eponymous syndrome, also known as nevoid basal cell carcinoma syndrome (NBCCS), is an autosomal dominant disorder Chromosome 9 is one of the 23 pairs of chromosomes in humans.People normally have two copies of this chromosome. Chromosome 9 spans about 136 million base pairs of nucleic acids (the building blocks of DNA) and represents between 4 and 4.5 percent of the total DNA in cells.. Identifying genes on each chromosome is an active area of genetic research. . Because researchers use different.

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Cancer Council would like to acknowledge the traditional custodians of the land on which we live and work. We would also like to pay respect to the elders past and present and extend that respect to all other Aboriginal people goltz syndrome wikipedia. By 24/10/2020 Category: Uncategorized 24/10/2020 Category: Uncategorize syndrome; neurocardiofacial-cutaneous syndromes such as Noonan syndrome, Costello syndrome, Gorlin Syndrome, (also known as schinzel syndrome Robinow syndrome Simpson-golabi-behmel syndrome Sotos syndrome Sturge-Weber syndrome Weaver syndrome... dysostosis Costello syndrome Encephalocraniocutaneous lipomatosis FG syndrome Hailermann-streiff. Sindrome di Gorlin Italia. 258 likes · 2 talking about this. Siamo persone con la sindrome di Gorlin, vorremmo diffondere il più possibile informazioni a riguardo e creare un punto di riferimento Select Page. goltz syndrome wikipedia. by | Oct 24, 2020 | Uncategorized | 0 comments | Oct 24, 2020 | Uncategorized | 0 comment

Cowden Syndrome (CS) More than 90% of individuals with CS have some clinical manifestation of the disorder by the late 20s [Nelen et al 1996, Eng 2000].By the fourth decade, 99% of affected individuals develop the mucocutaneous stigmata (primarily trichilemmomas and papillomatous papules) as well as acral and plantar keratoses. In addition, individuals with Cowden syndrome usually have. Hello! We notice that you are using Internet Explorer, which is not supported by Xenbase and may cause the site to display incorrectly. We suggest using a current version of Chrome, FireFox, or Safari ReportsWorldwide has announced the addition of a new report title Gorlin Syndrome (Basal Cell Nevus Syndrome) - Pipeline Review, H2 2017 to its growing collection of premium market research reports Permission is granted to copy, distribute and/or modify this document under the terms of the GNU Free Documentation License, Version 1.2 or any later version published by the Free Software Foundation; with no Invariant Sections, no Front-Cover Texts, and no Back-Cover Texts.A copy of the license is included in the section entitled GNU Free Documentation License Goltz-Gorlin Besides its formal name, it is most commonly referred to as Goltz-Gorlin syndrome, after Robert Goltz and Robert Gorlin . [11] Goltz and Gorlin worked together at Columbia University [12] and are credited for describing the symptoms of the disorder in more detail than ever before and tracking its genetic trends

Noonan syndrome with multiple lentigines - Wikipedi

Le syndrome de Goltz-Gorlin (ou hypoplasie dermique en aires) est une forme de polydysplasie ectodermique [1].C'est un syndrome génétique rare, caractérisé par une atteinte cutanée polymorphe et des anomalies très variées pouvant affecter les yeux, les dents, le squelette, le système nerveux central et les systèmes urinaires, gastro-intestinal et cardio-vasculair Gorlin syndrome. Nevoid basal-cell carcinoma syndrome (NBCCS), is an inherited medical condition involving defects within multiple body systems such as the skin, nervous system, eyes, endocrine system, and bones. People with this syndrome are particularly prone to developing a common and usually non-life-threatening form of non-melanoma skin. Some systemic disorders which may result in hypodontia include Crouzon syndrome, Ectodermal dysplasia, Ehlers-Danlos syndrome, and Gorlin syndrome. Abnormality in size. Microdontia is a condition where teeth are smaller than the usual size. Macrodontia is where teeth are larger than the usual size The pits look similar to large pores and can be more noticeable when the skin has absorbed water (like after a bath). The words palmar and plantar refer to the areas where they are found most often - on the palms of the hands and the bottoms of the feet. The usual caution applies: if [ People with Gorlin Syndrome have only 1 working copy of a gene involved in the Sonic Hedgehog Signalling Pathway; generally the gene called patched - 1 (PTCH1), but sometimes another of the relevant genes. Most people have 2 working copies of each of these genes, but Gorlin Syndrome results when one copy of a relevant gene is.

Gorlin syndrome: MedlinePlus Genetic

Gorlin sign the ability to touch the tip of the nose with the tongue, frequently a sign of Ehlers-Danlos syndrome.. Gorlin sign. Medical dictionary. 2011 Síndrome de Gorlin. El síndrome de Gorlin es una enfermedad hereditaria con participación de defectos dentro de múltiples sistemas del cuerpo. Involucra piel, sistema nervioso, ojos, sistema endocrino, y huesos. Es un trastorno poco frecuente que se incluye dentro de las enfermedades raras From Wikipedia the free encyclopedia In medicine, the Gorlin sign is the ability to touch the tip of the nose with the tongue . [1] Approximately ten percent of the general population can perform this act, whereas fifty percent of people with the inherited connective tissue disorder, Ehlers-Danlos syndrome , can Hennekam RCM, Allanson J, Krantz I Otopalatodigital syndrome. in Gorlin's Syndromes of the Head and Neck Fifth Edition 2010. Oxford University Press. JOURNAL ARTICLES Wade EM, Halliday BJ, Jenkins ZA, O'Neill AC, Robertson SP. The X-linked filaminopathies: Synergistic insights from clinical and molecular analysis

Goldenhar syndrome - Wikipedi

Rene Wiki is lid van Facebook. Magritte was born in Lessines, in the province of Hainaut. Enlarging Beast Gorlin (巨大化獣ゴルリン, Kyodaika-jū Gorurin): A giant white-skinned robot alien which absorbs and mimics the defeated Galactic Warriors Autres noms Causes Description. Le syndrome de Meier-Gorlin est une affection caractérisée principalement par une petite taille. Il est considéré comme une forme de nanisme primordial car le retard de croissance commence durant la vie intra-utérine Après la naissance, les individus affectés continuent de croître à un rythme lent. D'autres caractéristiques de cette condition sont des.

Gorlin Sendromu Nedir? Belirtileri, Nedenleri, Tedavis

Dan Gorlin is a video game programmer and designer best known for his 1982 Apple II game Choplifter. He also teaches and performs West African dance-drumming with Alokli West African Dance, an organization which Gorlin has directed since 1985 Gorlin syndrome is an autosomal dominant disorder that predisposes to basal cell carcinomas of the skin, ovarian fibromas, and medulloblastomas. Unlike other hereditary disorders associated with cancer, it features widespread developmental defects. To investigate the possibility that the syndrome is caused by mutation in a tumor suppressor gene. Goldenhar Syndrome: A rare congenital birth defect that causes abnormalities of facial development. also known asThis rare defect may occur as part of a syndrome or as an isolated abnormality. Type I: External portion of the ear is small in The isolated cause, a cause not associated with a syndrome, of anotia or microtia is not known, though it is believed to be of. Mutations in patients with Meier-Gorlin syndrome have Seckel syndrome. 210600. People with Seckel syndrome are noted to have microcephaly. Many also suffer from scoliosis, hip Meier-Gorlin syndrome. 224690. Individuals with Meier-Gorlin syndrome often have small ears and no kneecaps. They are also. Synonyms are: Aarskog-Ose-Pande syndrome; Lipodystrophy - Rieger anomaly - diabetes; Rieger anomaly-partial lipodystrophy syndrome. The first description comes from 1975 by the US human geneticist Robert J. Gorlin et al. And in the same year by the US pediatrician JA Sensenbrenner et al. The syndrome is not to be confused with short QT syndrome

Nevoid basal-cell carcinoma syndrome — Wikipedia

Many also suffer from scoliosis, hip Meier-Gorlin syndrome. 224690. Individuals with Meier-Gorlin syndrome often have small ears and no kneecaps. They are also Like Russell-Silver syndrome, they usually exceed the height of those with Seckel syndrome and ODPDI and II. It is also known. With Reverso you can find the French translation, definition or synonym for syndrome de Gorlin-Goltz and thousands of other words. You can complete the translation of syndrome de Gorlin-Goltz given by the French-English Collins dictionary with other dictionaries such as: Wikipedia, Lexilogos, Larousse dictionary, Le Robert, Oxford, Gréviss

Gorlin syndrome Other conditions Cancer Research U

Some subtypes of oral-facial-digital syndrome have similar limb malformations [ Gorlin et al ]. The gene encodes a protein of 1, amino acids. The Greig cephalopolysyndactyly syndrome. Greig cephalopolysyndactyly syndrome - Wikipedia. A markedly broad hallux visible increase in width of the hallux without an increase in the dorso-ventral. Gorlin cyst sign syndrome; Look at other dictionaries: Gorlin formula — a formula yielding an estimated area of the opening of a cardiac valve by calculating flow through the opening and pressure gradient across the valve.

Bixler-Christian-Gorlin syndrome Wikicure Wiki Fando

Define Basal Cell Nevus Syndrome. Basal Cell Nevus Syndrome synonyms, Basal Cell Nevus Syndrome pronunciation, Basal Cell Nevus Syndrome translation, English dictionary definition of Basal Cell Nevus Syndrome. n 1. a rare congenital disorder in which cancer destroys the facial skin and causes blindness; skeletal anomalies and some mental. Gordon Syndrome is a rare, inherited disorder that affects movement in the joints of the upper and lower limbs, also known as distal arthrogryposis.People with this disorder can be born with several fingers fixed in a flexed position (camptodactyly), clubfoot, and an opening in the roof of the mouth (cleft palate).Their joints are often very stiff or unable to move

Phelan McDermid Syndrome - Autism 3 year old Speech

Goldenhar Syndrome - EyeWik

A popliteal pterygium syndrome (PPS) is a very rare congenital disease with an inherited gene defect that the face, the limbs and the genital area concerned. The term PPS was coined by Gorlin in 1968 on the basis of the extremely rare malformation, the popliteal pterygium (an adhesion in the hollow of the knee) Seckel syndrome. 210600.People with Seckel syndrome are noted to have microcephaly.Many also suffer from scoliosis, hip Nelson de la Rosa - actor linked to the USA baseball team Boston Red Sox Meier-Gorlin syndrome. 224690.Individuals with Meier-Gorlin syndrome often have small ears and no kneecaps. They are also Like Russell-Silver syndrome, they usually exceed the height of those. Alerts and Notices Synopsis Basal cell nevus syndrome (BCNS, also known as Gorlin syndrome and nevoid basal cell carcinoma syndrome) is a rare condition that is usually inherited in an autosomal dominant fashion, although a high percentage of cases are sporadic. The majority of inherited cases are caused by PTCH1 gene mutations, but PTCH2 and SUFU mutations have also been found to be responsible Rieger syndrome is a rare genetic disorder characterized by absent or under-developed (hypodontia or partial adontia) teeth, mild craniofacial abnormalities, and various abnormalities of the eye, especially glaucoma. If unaccompanied by other signs and symptoms, the eye abnormalities are referred to as Rieger eye anomalies

Gorlin-Chaudhry-Moss Syndrome - NORD (National

Medullobastomas are associated with a number of syndromes that include Gorlin syndrome and Turcot syndrome. On gross pathology, a pink, solid, and well circumscribed mass is a characteristic finding of medulloblastoma. On microscopic histopathological analysis,. Gorlin-Goltz syndrome. Gorlin-Goltz syndrome or nevoid basal cell carcinoma syndrome (NBCCS) is a genetic condition which greatly increases the risk of developing BCCs.. A rare autosomal dominant condition that occurs as a result of gene mutation, specifically the PTCH1 gene.Individuals with Gorlin syndrome typically begin to develop BCCs during adolescence or early adulthood Popliteal pterygium syndrome (PPS) is an inherited condition affecting the face, limbs, and genitalia. The syndrome goes by a number of names including the popliteal web syndrome and, more inclusively, the facio-genito-popliteal syndrome. The term PPS was coined by Gorlin et al.. in 1968 on the basis of the most unusual anomaly, the popliteal pterygium (a web behind the knee) (pathology) A recognizable pattern of signs, symptoms and/or behaviours, especially of a disease or medical or psychological condition. Down syndrome; acquired immune deficiency syndrome; restless-leg syndrome; battered-wife syndrome 2013 May-June, Katie L. Burke, In the News, in American Scientist, volume 101, number 3, page 193: Bats host many.

File:Ovarian fibroma - high magFile:Ovarian fibroma - intermed magSkull with Leontiasis Ossea, also commonly known as “lionNoonans syndrom med flera lentigines - Noonan syndrome