GAPO SYNDROME IN TWO SIBLINGS
Abstract
We report two siblings, born out of a consanguineous marriage, presented with growth retardation, alopecia, unerupted teeth, persistent anterior fontanelle, large cornea and nystagmus. Imaging studies revealed delayed bone age, pseudo-anodontia, patent anterior fontanelle, hydrocephalus and hyperintense periventricular and deep white matter on T2 weighted MRI, pale optic disc on fundoscopy. Genetic tests revealed homozygous mutation in ANTXR1 gene in chromosome 2, confirming a diagnosis of GAPO (growth retardation, alopecia, pseudo-anodontia and optic atrophy) syndrome.
Keywords
Full Text:
PDFReferences
Tipton, R. E., & Gorlin, R. J. (1984). Growth retardation, Alopecia, Pseudo‐anodontia, and optic atrophy—The GAPO syndrome: Report of a patient and review of the literature. American journal of medical genetics, 19(2), 209-216.
Stránecký, V., Hoischen, A., Hartmannová, H., Zaki, M. S., Chaudhary, A., Zudaire, E., ... & Sovová, J. (2013). Mutations in ANTXR1 cause GAPO syndrome. The American Journal of Human Genetics, 92(5), 792-799.
Goloni‐Bertollo, E. M., Ruiz, M. T., Goloni, C. B. V., Muniz, M. P., Valério, N. I., & Pavarino‐Bertelli, É. C. (2008). GAPO syndrome: three new Brazilian cases, additional osseous manifestations, and review of the literature. American Journal of Medical Genetics Part A, 146(12), 1523-1529.
Lei, S., Iyengar, S., Shan, L., Cherwek, D. H., Murthy, S., & Wong, A. M. (2010). GAPO syndrome: a case associated with bilateral interstitial keratitis and hypothyroidism. Clinical dysmorphology, 19(2), 79-81.
Wajntal, A., Koiffmann, C. P., Mendonça, B. B., Sotto, M. N., & Rati, P. B. M. (1990). Gapo syndrome (mokusick 23074). A connective tissue disorder. Programa e Resumos.
Refbacks
- There are currently no refbacks.