Total: 2 |
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PMID (PMCID) | ||
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11152149 |
FEMALE | Infant, Newborn |
An Asian girl with a 'milder' form of the Hydrolethalus syndrome. | ||
Shotelersuk V, Punyavoravud V, Phudhichareonrat S, Kukulprasong A. Clin Dysmorphol. 2001;10(1):51-5. |
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Hydrolethalus syndrome is an autosomal recessive disorder characterized by hydrocephalus, micrognathia, limb anomalies and several other abnormalities, mostly in the midline structures. | ||
6390321 |
FEMALE | Infant, Newborn |
Hydrolethalus syndrome in consecutive African siblings. | ||
Adetoro OO, Komolafe F, Anjorin A. Pediatr Radiol. 1984;14(6):422-4. |
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Hydrolethalus syndrome may comprise mainly hydrocephalus, polydactyly, micrognathia, congenital cardiac and respiratory anomalies and uniform lethality. |