Bilateral persistent hyperplastic primary vitreous: An Egyptian family supporting a rare autosomal dominant inheritance

Genetic Counseling

Volumn 17, Issue 4, 2006, Pages 441-447

  Galal, Amany H ^a   Kotoury, A I S ^b   Azzab, A A ^a  

^a RESEARCH INSTITUTE OF OPHTHALMOLOGY   (Egypt)

^b NATIONAL RESEARCH CENTRE   (Egypt)

Author keywords

Autosomal dominant inheritance; Egypt; Persistent hyperplastic primary vitreous

Indexed keywords

ANAMNESIS; APHAKIA; ARTICLE; AUTOSOMAL DOMINANT INHERITANCE; CASE REPORT; CLINICAL FEATURE; ECHOOCULOGRAPHY; EGYPT; HUMAN; MALE; MICROPHTHALMIA; NYSTAGMUS; PERSISTENT HYPERPLASTIC PRIMARY VITREOUS; PHOTOSTIMULATION; PHYSICAL EXAMINATION; PIGMENT EPITHELIUM; PRESCHOOL CHILD; RARE DISEASE; VISUAL ACUITY;

CHILD, PRESCHOOL; CHROMOSOME DISORDERS; CONSANGUINITY; EGYPT; HUMANS; HYPERPLASIA; MALE; PEDIGREE; VITREOUS BODY;

EID: 33847280380     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

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