Evidence map›Paper›PMID 30881414›Full record

ArticlePakistan journal of medical sciences

Ambiguous genitalia: An overview of 7 years experience at the Children's Hospital & Institute of Child Health, Lahore, Pakistan.

Jaida Manzoor, Sommayya Aftab, Muhammad Yaqoob

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Article in Pakistan journal of medical sciences. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 6 papers.

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6citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

6 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Jaida ManzoorDr. Jaida Manzoor, MBBS, FCPS. Associate Professor (Pediatric Endocrinology), Department of Pediatric Endocrinology and Diabetes, The Children's Hospital & Institute of Child Health, Lahore, Pakistan.
Sommayya AftabDr. Sommayya Aftab, MBBS, FCPS. Senior Registrar (Pediatric Endocrinology), Department of Pediatric Endocrinology and Diabetes, The Children's Hospital & Institute of Child Health, Lahore, Pakistan.
Muhammad YaqoobDr. Muhammad Yaqoob, MBBS, MCPS, PhD. Assistant Professor (Clinical Genetics), Department of Genetics, The Children's Hospital & Institute of Child Health, Lahore, Pakistan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectiveTo determine the classification and etiological diagnosis of children presented with ambiguous genitalia/atypical genitalia according to the newer classification system of Disorder of Sex Development (DSD).

methodsThis observational, cross-sectional study was conducted at the Department of Pediatric Endocrinology and Diabetes at The Children's Hospital &Institute of Child Health, Lahore from January, 2007 to December; 2014. Files of all the children with ambiguous genitalia were retrospectively analyzed and relevant data was retrieved. All the information was recorded on predesigned proforma and analyzed accordingly.

resultsA total of 300 cases of ambiguous genitalia classified according to the new DSD classification. 46, XX DSD were 54.3% (n=163), 46, XY DSD were 43.7% (n=131), sex chromosome DSD were 2% (n=6). Among 46, XX DSD cases, the most common cause was congenital adrenal hyperplasia (97%, n=158). However, in 46, XY DSD partial androgen insensitivity/

conclusionAmbiguous genitalia have varied etiologies, 46; XXDSD found being the commonest of all, showing predominance of CAH especially salt loosing type. The early detection and prompt treatment of cases of ambiguous genitalia plays a pivotal role in the management of acute life threatening condition and gender assignment.

Indexed as

Ambiguous genitaliaCongenital Adrenal HyperplasiaDisorder of Sex Development

Identifiers

PMID30881414
PMCPMC6408627

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.