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Odontotrichomelic syndrome
rareOdontotrichomelic syndrome is characterized by malformations of all four extremities, hypoplastic nails, ear anomalies, hypotrichosis, abnormal dentition, hyperhidrosis and nasolacrimal duct obstruction. So far, it has been described in less than 10 patients. Transmission is autosomal recessive.
- Identifiers
- MONDO:0010111 OMIM:273400Orphanet:2723
- Part of
- Ectodermal dysplasia syndrome
- Also known as
- Freire-Maia odontotrichomelic syndrome · Freire-Maia syndrome · odontotrichomelic hypohidrotic dysplasia · tetramelic deficiencies, ectodermal dysplasia, deformed ears, and other abnormalities
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