obsolete_Bartsocas-Papas syndrome true Replaced with Mondo term. Lethal popliteal pterygium syndrome 3.41.0 OMIM:263650 orphanet Bartsocas-Papas syndrome is a rare, inherited, popliteal pterygium syndrome (see this term) characterized by microcephaly, severe popliteal webbing, oligosyndactyly, genital abnormalities, a typical face with short palpebral fissures, ankyloblepharon, hypoplastic nose, filiform bands between the jaws and facial clefts, and other 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. Autosomal recessive popliteal pterygium syndrome http://purl.obolibrary.org/obo/MONDO_0009901 ICD10:Q87.2