The use of fluorescence in situ hybridization in the diagnosis of hidden mosaicism: apropos of three cases of sex chromosome anomalies

Autor(es)

Maciel-Guerra, Andrea Trevas ; De Paulo, Juliana ; Santos, Ana Paula ; Guaragna-Filho, Guilherme ; Ribeiro Andrade, Juliana Gabriel ; Siviero-Miachon, Adriana Aparecida ; Spinola-Castro, Angela Maria ; Guerra-Junior, Gil

• Tipo de documento: Artigo Científico
• Fonte: Arquivos Brasileiros de Endocrinologia e Metabologia; v. 56, n. 8, p. 7-pg., 2012-11-01.

Resumo

FISH has been used as a complement to classical cytogenetics in the detection of mosaicism in sex chromosome anomalies. The aim of this study is to describe three cases in which the final diagnosis could only be achieved by FISH. Case 1 was an 8-year-old 46, XY girl with normal female genitalia referred to our service because of short stature. FISH analysis of lymphocytes with probes for the X and Y centromeres identified a 45, X/46, X, idic(Y) constitution, and established the diagnosis of Turner syndrome. Case 2 was a 21-month-old 46, XY boy with genital ambiguity (penile hypospadias, right testis, and left streak gonad). FISH analysis of lymphocytes and buccal smear identified a 45, X/46, XY karyotype, leading to diagnosis of mixed gonadal dysgenesis. Case 3 was a 47, XYY 19-year-old boy with delayed neuromotor development, learning disabilities, psychological problems, tall stature, small testes, elevated gonadotropins, and azoospermia. FISH analysis of lymphocytes and buccal smear identified a 47, XYY/48, XXYY constitution. Cases 1 and 2 illustrate the phenotypic variability of the 45, X/46, XY mosaicism, and the importance of detection of the 45, X cell line for proper management and follow-up. In case 3, abnormal gonadal function could be explained by the 48, XXYY cell line. The use of FISH in clinical practice is particularly relevant when classical cytogenetic analysis yields normal or uncertain results in patients with features of sex chromosome aneuploidy. Arq Bras Endocrinol Metab. 2012;56(8):545-51 (AU)

• Processo FAPESP: 11/50189-7 - Estudo clínico, citogenético, e pesquisa de microdeleções do cromossomo Y em indivíduos com disgenesias testiculares mista e parcial 46,XY
• Beneficiário: Andrea Trevas Maciel Guerra
• Modalidade de apoio: Auxílio à Pesquisa - Regular