Bartsocas-Papas syndrome is a rare, inherited, popliteal pterygium syndrome (see this term) characterized by severe popliteal webbing, microcephaly, a typical face with short 
palpebral fissures, ankyloblepharon, hypoplastic nose, filiform bands between 
the jaws and facial 
clefts, oligosyndactyly, genital abnormalities, and additional ectodermal anomalies (i.e. absent 
hair, eyebrows, lashes, nails). It is often fatal 
in the neonatal period, but patients living 
until childhood have been reported.
Without darkness, one cannot know the light 
Slavshit
Sandshit
Jump in the discussion.
No email address required.
What's the oldest one of these has gotten
Jump in the discussion.
No email address required.
Most are gone by the age of 2 (under 20 months seems to be the vast majority of the ones who survive the neonatal period), but I saw 2 cases that reported a chld still undergoing treatment at the age of 4 and another report of a child
making it to 6, but those cases are not confirmed (to my knowledge).
Without darkness, one cannot know the light
Jump in the discussion.
No email address required.
More options
Context
More options
Context