Oculo-palato-cerebral syndrome: A third case supporting autosomal recessive inheritance

American Journal of Medical Genetics

Volumn 130 A, Issue 1, 2004, Pages 92-95

  Alanay, Yasemin ^a   Boduroǧlu, Koray ^a   Sönmez, Bariş ^a   Orhan, Mehmet ^a  

^a HACETTEPE UNIVERSITY   (Turkey)

Author keywords

Autosomal recessive; Cleft palate; Microphthalmia; Oculo palato cerebral syndrome; Persistent hyperplastic primary vitreous

Indexed keywords

AUTOSOMAL RECESSIVE INHERITANCE; CASE REPORT; CLEFT PALATE; CLINICAL EXAMINATION; CONFERENCE PAPER; FEMALE; HUMAN; INFANT; MALFORMATION SYNDROME; MICROPHTHALMIA; OCULOPALATOCEREBRAL SYNDROME; PEDIGREE; PRIORITY JOURNAL;

GENETTA;

EID: 4344690680     PISSN: 15524825     EISSN: None     Source Type: Journal    
DOI: 10.1002/ajmg.a.30114     Document Type: Conference Paper

References (6)

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3. Lin AE, Biglan AW, Garver KL. 1990. Persistent hyperplastic primary vitreous with vertical transmission. Ophthalmic Paediatr Genet 11: 121-122.
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5. Pellegrino JE, Engel JM, Chavez D, Day-Salvatore D. 2001. Oculopalatal-cerebral syndrome: A second case. Am J Med Genet 99:200-203.
6. Wang NK, Philips CI. 1973. Persistent hyperplastic primary vitreous in nonidentical twins. Acta Ophthamol 51:434-437.