Long-Term Follow-Up of Patients with 46,XY Partial Gonadal Dysgenesis Reared as Males
Background/Aims. Studies on 46,XY partial gonadal dysgenesis (PGD) have focused on molecular, gonadal, genital, and hormone features; little is known about follow-up. Our aim was to analyze long-term outcomes of PGD. Methods. Retrospective longitudinal study conducted at a reference service in Brazi...
Saved in:
Main Authors: | Juliana Gabriel Ribeiro de Andrade, Antonia Paula Marques-de-Faria, Helena Campos Fabbri, Maricilda Palandi de Mello, Gil Guerra-Júnior, Andréa Trevas Maciel-Guerra |
---|---|
Format: | Article |
Language: | English |
Published: |
Wiley
2014-01-01
|
Series: | International Journal of Endocrinology |
Online Access: | http://dx.doi.org/10.1155/2014/480724 |
Tags: |
Add Tag
No Tags, Be the first to tag this record!
|
Similar Items
-
Clinical and Laboratorial Features That May Differentiate 46,XY DSD due to Partial Androgen Insensitivity and 5α-Reductase Type 2 Deficiency
by: Nélio Neves Veiga-Junior, et al.
Published: (2012-01-01) -
46, XY Complete Gonadal Dysgenesis (Swyer Syndrome) Presenting as Primary Amenorrhea in a Normomorphic Adult Female From Kakamega, Kenya
by: Christian Omoaghe
Published: (2025-01-01) -
Combination of Gonadal Dysgenesis and Monosomy X with a Novo Translocation (13,14)
by: Hanane Latrech, et al.
Published: (2018-01-01) -
Behavioural Problems in Children with 46XY Disorders of Sex Development
by: Nalini M. Selveindran, et al.
Published: (2017-01-01) -
Congenital Lipoid Adrenal Hyperplasia, as a Poorly Understood Cause of 46 XY Sexual Differentiation Disorder
by: Raúl Villanueva Rodríguez, et al.
Published: (2024-01-01)