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Triophthalmia and facial clefting: a case report.

ABSTRACT: We describe a Libyan boy with an unusual phenotype of multiple congenital anomalies, including triophthalmia, dolichocephaly, porencephaly, cleft lip/palate, facial asymmetry, micrognathia, and VSD. The reported phenotype is likely to represent a new entity of non-chromosomal syndromic triophthalmia. Other possibilities are discussed.

SUBMITTER: Tayel SM

PROVIDER: S-EPMC1051469 | biostudies-other | 1998 Oct

REPOSITORIES: biostudies-other

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Triophthalmia and facial clefting: a case report.

Tayel S M SM Sabry M A MA Kader N A NA Farah S S Al-Awadi S A SA Farag T I TI

Journal of medical genetics 19981001 10

We describe a Libyan boy with an unusual phenotype of multiple congenital anomalies, including triophthalmia, dolichocephaly, porencephaly, cleft lip/palate, facial asymmetry, micrognathia, and VSD. The reported phenotype is likely to represent a new entity of non-chromosomal syndromic triophthalmia. Other possibilities are discussed. ...[more]

PMID: 9783717

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