Please use this identifier to cite or link to this item: https://hdl.handle.net/20.500.12104/40298
Title: Congenital hypertrichosis, osteochondrodysplasia, and cardiomegaly: Further delineation of a new genetic syndrome
Author: García-Cruz, D.
Sanchez-Corona, J.
Nazara, Z.
García-Cruz, M.O.
Figuera, L.E.
Castaneda, V.
Cantu, J.M.
Issue Date: 1997
Abstract: The hypertrichosis and osteochondrodysplasia syndrome is a rare entity with clinical findings including macrosomia at birth cardiomegaly. Autosomal recessive inheritance is presumed based on the report of two affected sibs born to healthy parents. Here we report on four new patients with their follow-up data, as well as on one of the four cases from the original report. Comparison of all eight cases indicates that they share 50% of clinical and radiological changes. This report contributes to the further delineation of this newly recognized syndrome.
URI: http://hdl.handle.net/20.500.12104/40298
http://www.scopus.com/inward/record.url?eid=2-s2.0-0031048676&partnerID=40&md5=62e4fb4e74c5ed17bad6f84fe0a2f882
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