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Bookmark or Share- hydrolethalus syndrome - National Organization for Rare DisordersHydrolethalus (HLS) is a severe fetal malformation syndrome characterized by craniofacial dysmorphic features, central nervous system, cardiac, respiratory tract and limb abnormalities.
- Hydrolethalus syndrome - thefetus.netDefinition: This syndrome is characterized by multiple developmental defects of fetus as polydactyly (postaxial in the hands and preaxial in the feet), central nervous system malformation such as hydrocephalus and absent midline structures of the brain, micrognathia, limb anomalies and several other abnormalities, mostly in the midline structures.
- Hydrolethalus syndrome - WikipediaHydrolethalus syndrome (HLS) is a rare genetic disorder that causes improper fetal development, resulting in birth defects and, most commonly, stillbirth. [1] HLS is associated with HYLS1 mutations. The gene encoding HYLS1 is responsible for proper cilial development within the human body.
- Hydrolethalus syndrome | Myriad Foresight® Carrier ScreenWhat is Hydrolethalus Syndrome? Hydrolethalus syndrome is an inherited disease caused by harmful genetic changes (mutations) in the HYSF1 gene. The HYSF1 gene plays an important role in fetal development. Hydrolethalus syndrome causes severe brain abnormalities.
- Hydrolethalus Syndrome - Encyclopedia.comHydrolethalus syndrome is a condition that causes improper fetal development. Multiple malformations along the body's midline, such as heart and brain defects, a cleft lip or palate, an abnormally shaped nose or jaw, and incomplete lung development result from this syndrome.
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