Literature DB >> 30803928

A clinical algorithm to diagnose differences of sex development.

Nayla Y León1, Alejandra P Reyes2, Vincent R Harley3.   

Abstract

The diagnosis and management of children born with ambiguous genitalia is challenging for clinicians. Such differences of sex development (DSDs) are congenital conditions in which chromosomal, gonadal, or anatomical sex is atypical. The aetiology of DSDs is very heterogenous and a precise diagnosis is essential for management of genetic, endocrine, surgical, reproductive, and psychosocial issues. In this Review, we outline a step-by-step approach, compiled in a diagnostic algorithm, for the clinical assessment and molecular diagnosis of a patient with ambiguity of the external genitalia on initial presentation. We appraise established and emerging technologies and their effect on diagnosis, and discuss current controversies.
Copyright © 2019 Elsevier Ltd. All rights reserved.

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Year:  2019        PMID: 30803928     DOI: 10.1016/S2213-8587(18)30339-5

Source DB:  PubMed          Journal:  Lancet Diabetes Endocrinol        ISSN: 2213-8587            Impact factor:   32.069


  6 in total

Review 1.  Towards improved genetic diagnosis of human differences of sex development.

Authors:  Emmanuèle C Délot; Eric Vilain
Journal:  Nat Rev Genet       Date:  2021-06-03       Impact factor: 53.242

Review 2.  Diverse Regulation but Conserved Function: SOX9 in Vertebrate Sex Determination.

Authors:  Brittany Vining; Zhenhua Ming; Stefan Bagheri-Fam; Vincent Harley
Journal:  Genes (Basel)       Date:  2021-03-26       Impact factor: 4.096

3.  Clinical, Etiological and Laboratory Profile of Children with Disorders of Sexual Development (DSD)-Experience from a Tertiary Pediatric Endocrine Unit in Western India.

Authors:  Rahul Jahagirdar; Vaman Khadilkar; Ruma Deshpande; Nikhil Lohiya
Journal:  Indian J Endocrinol Metab       Date:  2021-07-21

4.  Patients with disorders of sex development.

Authors:  Renata Markosyan
Journal:  Ann Pediatr Endocrinol Metab       Date:  2021-06-30

Review 5.  A novel missense heterozygous mutation in MAP3K1 gene causes 46, XY disorder of sex development: case report and literature review.

Authors:  Aisha Al Shamsi; Noura Al Hassani; Moustafa Hamchou; Raya Almazrouei; Aziz Mhanni
Journal:  Mol Genet Genomic Med       Date:  2020-09-28       Impact factor: 2.183

6.  46, XX Ovotesticular disorder of sex development (true hermaphroditism) with seminoma: A case report.

Authors:  Zixiang Li; Junjie Liu; Yunpeng Peng; Renfu Chen; Peng Ge; Junqi Wang
Journal:  Medicine (Baltimore)       Date:  2020-10-02       Impact factor: 1.817

  6 in total

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