DHX37 and the implications in Disorders of Sex Development: an update review

FR de Oliveira, MS Guaragna, AT Maciel-Guerra… - Horm Res …, 2023 - karger.com
Background: DHX37 is an autosomal gene responsible for encoding a helicase from the
DExD/H-box family that plays an essential role in ribosome biogenesis. Variants in this gene …

[HTML][HTML] Virilization at puberty in adolescent girls may reveal a 46, XY disorder of sexual development

A Bergougnoux, L Gaspari, M Soleirol… - Endocrine …, 2023 - ec.bioscientifica.com
Objective: Although hyperandrogenism is a frequent cause of consultation in adolescent
girls, more severe forms with virilization must lead to suspect an adrenal or ovarian tumor …

Identification and functional analysis of a rare variant of gene DHX37 in a patient with 46,XY disorders of sex development

W Jiang, J Yu, Y Mao, Y Tang, L Cao… - … Genetics & Genomic …, 2024 - Wiley Online Library
Abstract Background 46, XY sex reversal 11 (SRXY11)[OMIM# 273250] is characterized by
genital ambiguity that may range from mild male genital defects to gonadal sex reversal in …

DHX37 Variant is One of Common Genetic Causes in Japanese Patients with Testicular Regression Syndrome/Partial Gonadal Dysgenesis without Müllerian …

K Shimura, Y Ichihashi, S Nakano, T Sato… - Hormone Research in …, 2024 - karger.com
Introduction: The testicular regression syndrome (TRS) is a form of differences of sex
development (DSD) in which the testes differentiate and function during early embryonic …

Phenotype‐Genotype Discordance and a Case of a Disorder of Sexual Differentiation

M Snipes, S Stokes, A Vidalin, LD Moore… - Case Reports in …, 2024 - Wiley Online Library
Discordance between the genetic sex and phenotype seen on ultrasound can identify
disorders of sexual development (DSD) that previously escaped detection until puberty. We …

DHX37 and the implications in Disorders of Sex Development: an update

FR de Oliveira, MS Guaragna, AT Maciel-Guerra… - 2023 - karger.com
Background: DHX37 is an autosomal gene responsible for encoding a helicase from the
DExD/H-box family that plays an essential role in ribosome biogenesis. Variants in this gene …

DHX37 Variant Is One of the Common Genetic Causes in Japanese Patients with Testicular Regression Syndrome/Partial Gonadal Dysgenesis without Müllerian …

KSYIS Nakanoa, T Satoa, THKNS Narumia… - 2024 - karger.com
Introduction: The testicular regression syndrome (TRS) is a form of differences of sex
development (DSD) in which the testes differentiate and function during early embryonic …