Evidence map›Paper›PMID 41920275›Full record

SynthesisEndocrine2026

3β-Hydroxysteroid dehydrogenase type-2 deficiency: Our experience and gonadal function-focused systematic review.

Aaditya Daga, Aditya Phadte, Manjiri Karlekar, Vijaya Sarathi, Anurag Ranjan Lila, Samiksha Hegishte, Saba Samad Memon, Rohit Barnabas, Nalini Shah, Shriraam Mahadevan and 1 more

Abstract readSystematic Review
PubMed Publisher
In one paragraph

Synthesis in Endocrine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

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4 · The record

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5 · Who and what money

Authors and funding

11 authors.

Aaditya DagaDepartment of Endocrinology and Metabolism, King Edward Memorial Hospital and Seth Gordhandas Sunderdas Medical College, Mumbai, India.
Aditya PhadteDepartment of Endocrinology and Metabolism, King Edward Memorial Hospital and Seth Gordhandas Sunderdas Medical College, Mumbai, India.
Manjiri KarlekarDepartment of Endocrinology and Metabolism, King Edward Memorial Hospital and Seth Gordhandas Sunderdas Medical College, Mumbai, India.
Vijaya SarathiDepartment of Endocrinology, Vydehi Institute of Medical Sciences and Research Centre, Bangalore, India.
Anurag Ranjan LilaDepartment of Endocrinology and Metabolism, King Edward Memorial Hospital and Seth Gordhandas Sunderdas Medical College, Mumbai, India. anuraglila@kem.edu.ORCID 0000-0002-9623-4471
Samiksha HegishteDepartment of Endocrinology and Metabolism, King Edward Memorial Hospital and Seth Gordhandas Sunderdas Medical College, Mumbai, India.
Saba Samad MemonDepartment of Endocrinology and Metabolism, King Edward Memorial Hospital and Seth Gordhandas Sunderdas Medical College, Mumbai, India.
Rohit BarnabasDepartment of Endocrinology and Metabolism, King Edward Memorial Hospital and Seth Gordhandas Sunderdas Medical College, Mumbai, India.
Nalini ShahDepartment of Endocrinology and Metabolism, King Edward Memorial Hospital and Seth Gordhandas Sunderdas Medical College, Mumbai, India.
Shriraam MahadevanSri Ramachandra Institute of Higher Education and Research, Chennai, India.
Tushar BandgarDepartment of Endocrinology and Metabolism, King Edward Memorial Hospital and Seth Gordhandas Sunderdas Medical College, Mumbai, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeIn 3β-Hydroxysteroid dehydrogenase type-2 (3β-HSD2) deficiency, the gonadal phenotypic spectrum and its correlation with genotype are unclear. We describe our center’s experience and perform a systematic review.

methodsRetrospective record review of five 3β-HSD2 deficiency probands from our center, along with per-patient data analysis of reported probands, was conducted to understand the genotype and gonadal phenotype correlation. Probands were subgrouped based on karyotype and residual enzyme activity (REA) of the genetic variant.

resultsOf 128 probands, subgroups were: 46,XY REA ≤ 2% (n = 66), > 2% (n = 21); 46,XX REA ≤ 2% (n = 29), > 2% (n = 12). All 46,XY probands had atypical genitalia; Sinnecker score ≤ 3 (93.1% vs. 88.2%) and cryptorchidism (13.7% vs. 23.5%) were similar between REA ≤ 2% and > 2% groups. 46,XY probands with pubertal data (REA ≤ 2%: 11, > 2%: 3) all had spontaneous puberty (gynecomastia: 3; early puberty: 2) with normal testosterone and gonadotropins (except two). Testicular adrenal rest tumors (TARTs) were reported in seven (median age 13 years); some retained spermatogenesis, and one case documented paternity. No testicular germ-cell tumors were reported. 46,XX probands with pubertal data (REA ≤ 2%: 12, > 2%: 4), all had spontaneous puberty except one (pubertal arrest). Median ages at thelarche (9.0 vs. 9.5 years) and menarche (12 vs. 11.5 years) were comparable between REA groups. Polycystic ovarian morphology (PCOM) was reported in seven, and infertility in one.

conclusionNo clear genotype–gonadal phenotype correlation was observed. Pubertal development and hormone secretion are largely preserved irrespective of REA. TARTs and PCOM are not uncommon. Fertility potential requires further studies.

Indexed as

17-Hydroxysteroid DehydrogenasesAdolescentAdultChildChild, PreschoolFemaleGenotypeHumansMalePhenotypeProgesterone ReductasePubertyRetrospective Studies17-Hydroxysteroid Dehydrogenases3 beta-hydroxysteroid dehydrogenase type IIProgesterone Reductase3β-Hydroxysteroid dehydrogenaseCongenital adrenal hyperplasiaGonadal function

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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.