CODAS syndrome: A new distinct MCA/MR syndrome with radiological changes of spondyloepiphyseal dysplasia. Another case report

We report on a young girl with psychomotor delay, cataracts, abnormally shaped teeth, malformed ears, and radiological findings of spondylo‐epiphyseal dysplasia. The clinical picture resembles the CODAS syndrome described by Shebib et al. [Am J Med Genet 40:88–93, 1991]. © 1995 Wiley‐Liss, Inc....

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Veröffentlicht in:	American journal of medical genetics 1995-01, Vol.55 (1), p.19-20
Hauptverfasser:	de Almeida, José Carlos Cabral, Vargas, Fernando Regla, Barbosa-Neto, João G., Llerena Jr, Juan C.
Format:	Artikel
Sprache:	eng
Schlagworte:	Abnormalities, Multiple - diagnostic imaging Abnormalities, Multiple - genetics Biological and medical sciences Child, Preschool Complex syndromes dental anomalies eye anomalies Female Humans MCA/MR syndrome Medical genetics Medical sciences Osteochondrodysplasias - diagnostic imaging Osteochondrodysplasias - genetics Radiography skeletal anomalies
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Zusammenfassung:	We report on a young girl with psychomotor delay, cataracts, abnormally shaped teeth, malformed ears, and radiological findings of spondylo‐epiphyseal dysplasia. The clinical picture resembles the CODAS syndrome described by Shebib et al. [Am J Med Genet 40:88–93, 1991]. © 1995 Wiley‐Liss, Inc.
ISSN:	0148-7299 1096-8628
DOI:	10.1002/ajmg.1320550107