Universidad Complutense de Madrid
E-Prints Complutense

Clinical Variability of Primary Congenital Glaucoma in a Spanish Family With Cyp1b1 Gene Mutations

Impacto

Downloads

Downloads per month over past year

Morales Fernández, Laura and Martínez de la Casa, Jose Maria and García Bella, Javier and Méndez García, Carmen and Saenz Frances, Federico and García Antón, Maite and Escribano, Julio and García Feijoo, Julián (2015) Clinical Variability of Primary Congenital Glaucoma in a Spanish Family With Cyp1b1 Gene Mutations. Journal of Glaucoma, 24 (8). pp. 630-634. ISSN 1057-0829

[img] PDF
Restringido a Repository staff only

210kB

Official URL: http://dx.doi.org/10.1097/IJG.0000000000000067



Abstract

Background: Primary congenital glaucoma (PCG) is a rare disease. In around a third of Spanish patients, the disease is attributed to mutations in the CYP1B1 gene inherited in an autosomal recessive manner. Such mutations are the main known genetic cause of PCG.
Case Report: We describe the case of a family with 3 of 7 siblings diagnosed with PCG. In a genetic study of the CYP1B1 gene, 2 null mutations were identified in the affected siblings (R355fsX69/T404fsX38). Two of the 4 healthy siblings were heterozygous for mutation R355fsX69 and the remaining 2 had no mutations. The healthy parents were found to be heterozygous for mutations T404fsX38 (mother) and R355fsX69 (father). High variation in the expression of PCG was observed, especially in terms of disease onset and severity: Patient 1 in the eldest affected sibling, PCG was diagnosed at 8 years of age and is presently stable after 60 months of medical treatment; patient 2 the second affected child underwent surgery at 7 days of age. Today, at 104 months, she has undergone 2 operations on the right eye and 3 on the left eye; patient 3 the youngest sibling, the disease also manifested at birth and the boy underwent surgery at 4 days. Currently he is 84 months old, he has required 7 operations for glaucoma, 3 in the right eye and 4 in the left.
Conclusions: This clinical case reveals the etiological relationship between CYP1B1 mutations and PCG. In addition, it indicates a highly variable clinical picture associated with a single disease genotype mainly affecting disease onset and progression.


Item Type:Article
Additional Information:

Received May 15, 2013; Accepted March 11, 2014

Uncontrolled Keywords:Primary congenital glaucoma, CYP1B1 gene, Genotype-phenotype
Subjects:Medical sciences > Medicine > Ophtalmology
Medical sciences > Biology > Genetics
ID Code:41220
Deposited On:22 Feb 2017 09:38
Last Modified:22 Feb 2017 09:38

Origin of downloads

Repository Staff Only: item control page