Síndrome de morris associado à síndrome de hiperplasia adrenal congênita – diagnóstico fetal: relato de caso

Valdivina Eterna Falone; Waldemar Naves Amaral; Waldemar Naves Amaral Filho; Jonatha Fonseca Lopes; Thaynara Moraes Pacheco; Rafael Rocha Luzini; Juscelia Rodrigues Teles

Morris syndrome associated with congenital adrenal hyperplasia fetal diagnosis

case report

Authors

Valdivina Eterna Falone Clínica Fértile
Waldemar Naves do Amaral Clínica Fértile; Universidade Federal de Goiás
Waldemar Naves do Amaral Filho Universidade Federal de Goiás
Jonatha Fonseca Lopes Universidade Federal de Goiás
Thaynara de Moraes Pacheco Universidade Federal de Goiás
Rafael Rocha Luzini Universidade Federal de Goiás
Juscelia Rodrigues Teles Faculdade Alfredo Nasser

Keywords:

morris syndrome, fetal diagnosis, ultrasonography

Abstract

Ambiguous genitalia (AG) occurs due to dysfunctions in the genetic and hormonal signaling of the structures that make up the genitalia, forming part of the sexual development anomalies (SDA). We report a case of genital ambiguity in a patient with peripheral insensitivity to androgens (Morris Syndrome) and congenital adrenal hyperplasia, which was diagnosed through the association of ultrasonography with cordocentesis. Early diagnosis avoids severe psychosocial adversities for the patient and family.

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Published

2018-09-01

How to Cite

Falone VE, Amaral WN, Amaral Filho WN, Lopes JF, Moraes Pacheco T, Luzini RR, et al. Morris syndrome associated with congenital adrenal hyperplasia fetal diagnosis: case report. RBUS [Internet]. 2018 Sep. 1 [cited 2025 Jan. 18];(25):66-8. Available from: https://revistarbus.sbus.org.br/rbus/article/view/186