73 top medical experts on Lethal Type Popliteal Pterygium Syndrome across 7 countries and 3 U.S. states, including 6 MDs (Physicians). This is based on an objective analysis of their Scientific Publications, Clinical Trials, Medicare, and NIH Grants.
- Lethal Type Popliteal Pterygium Syndrome: 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.
- Clinical guidelines are the recommended starting point to understand initial steps and current protocols in any disease or procedure:
- Synonyms: Aslan Multiple Pterygium Syndrome, Bartsocas-Papas Syndrome, Aslan Type Multiple Pterygium Syndrome, Lethal Type Popliteal Pterygium
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