Hydrolethalus syndrome (less commonly referred to as Salonen-Herva-Norio syndrome) is a rare genetic disorder that causes improper fetal development, resulting in ...
236680 - HYDROLETHALUS SYNDROME 1; HLS1 ... NOTE: OMIM is intended for use primarily by physicians and other professionals concerned with ...
Information about hydrolethalus syndrome, a genetic disorder, including its symptoms and diagnosis.
A collection of disease information resources and questions answered by our Genetic and Rare Diseases Information Specialists for Hydrolethalus syndrome
Salonen R, Herva R, Norio R. The hydrolethalus syndrome: delineation of a "new", lethal malformation syndrome based on 28 patients. Clin Genet.
Hydrolethalus syndrome information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.
The official name of this gene is “hydrolethalus syndrome 1.” HYLS1 is the gene's official symbol. The HYLS1 gene is also known by other names, listed ...
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Hydrolethalus syndrome is a rare lethal genetic syndrome characterised by multiple developmental defects of fetus which include midline malformations
Hydrolethalus Syndrome 2 disease: Malacards - Research Articles, Symptoms, Drugs, Genes, Clinical Trials