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Genetic study of primary congenital glaucoma in Sharkia
Zagazig Medical Association Journal. 1990; 3 (3): 95-112
in English | IMEMR | ID: emr-18692
ABSTRACT
This study included 20 normal subjects as a control group and 20 cases suffering from primary congenital glaucoma. There were 4 familial cases, 4 cases with other ocular and systemic anomalies, 6 cases exposed to prenatal environmental factors and consanguinity was detected in 9 cases. Karyotyping revealed chromosomal anomalies in 3 cases of primary congenital glaucoma, this was in the form of chromatoid breaks in 2 cases and trisomy 13 in one case. All the 3 cases were exposed to prenatal environmental factors and have other ocular and systemic anomalies. Pedigrees analysis revealed that primary congenital glaucoma was inherited as multifactorial mode of inheritance
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Index: IMEMR (Eastern Mediterranean) Main subject: Blindness / Genetics / Intraocular Pressure Language: English Journal: Zagazig Med. Assoc. J. Year: 1990

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Index: IMEMR (Eastern Mediterranean) Main subject: Blindness / Genetics / Intraocular Pressure Language: English Journal: Zagazig Med. Assoc. J. Year: 1990