Popliteal pterygium syndrome, shortened to PPS, is a rare inherited genetic disorder marked by distinctive features of the face and skull, the muscles and bones, and the genitourinary system. It is mainly caused by a mutation of the IRF6 gene and follows an autosomal dominant pattern of inheritance. Typical features include webbing of skin behind the knee, cleft lip or palate and fused fingers or toes, and the severity and mix of features vary between affected people. The source gives an approximate incidence of 1 in every 300,000 live births. Trelat first described the condition in 1869, and Gorlin and colleagues named it in 1968. The word pterygium comes from the Greek word for wing, referring to the wing-like folds of tissue often seen.
Facts
Classification
Communicable or Non-communicable Transmission Route First Described Prevalence Band Causative Agent
Causative Agent (category) Sources
1. Monarch Initiative: popliteal pterygium syndrome - Monarch Initiative MONDO:0017435
Monarch InitiativeDisease descriptionQuote, Disease description
A rare, autosomal dominant inherited syndrome caused by mutations in the IRF6 gene.
View the Source 2. MedlinePlus Genetics (U.S. National Library of Medicine): Popliteal pterygium syndrome - MedlinePlus Genetics
MedlinePlus Genetics (U.S. National Library of Medicine)Description and InheritanceQuote, Description and Inheritance
This condition is inherited in an autosomal dominant pattern , which means one copy of the altered gene in each cell is sufficient to cause the disorder.
View the Source 3. Popliteal pterygium syndrome (Wikipedia)
Lead paragraph
rare inherited genetic disorder
Lead paragraph [first-described-year]
first described by Trélat in 1869
View the Source4. Orphadata (Orphanet): Orphadata: Epidemiology of rare diseases (en_product9_prev)
Orphadata (Orphanet)ORPHA:294963Quote, ORPHA:294963
Prevalence at birth Value and class 1-9 / 1 000 000
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