Luteinizing hormone β‐subunit deficiency: Report of a novel <i>LHB</i> likely pathogenic variant and a systematic review of the published literature-Reference-Cited by-同舟云学术

Luteinizing hormone β‐subunit deficiency: Report of a novel LHB likely pathogenic variant and a systematic review of the published literature

Published:2022-05-04 Issue:3 Volume:98 Page:383-393
ISSN:0300-0664
Container-title:Clinical Endocrinology
language:en
Short-container-title:Clinical Endocrinology

Author:

Barnabas Rohit¹,Jadhav SwatiRamteke²,Arya Sneha¹,Lila Anurag Ranjan¹^ORCID,Sarathi Vijaya³,Shah Gaurang R.⁴,Bhandare Vishwambhar V.⁵,Shah Nalini S.¹,Kunwar Ambarish⁵^ORCID,Bandgar Tushar¹^ORCID

Affiliation:

1. Department of Endocrinology Seth G. S. Medical College & KEM Hospital Mumbai India

2. Department of Endocrinology Sapthagiri Institute of Medical Sciences and Research Center Bangalore India

3. Department of Endocrinology Vydehi Institute of Medical Sciences and Research Centre Bangalore India

4. Department of Urology Saifee Hospital Mumbai India

5. Department of Biosciences and Bioengineering Indian Institute of Technology Bombay, Powai Mumbai India

Publisher

Wiley

Subject

Endocrinology, Diabetes and Metabolism,Endocrinology

Link

https://onlinelibrary.wiley.com/doi/pdf/10.1111/cen.14749

Reference26 articles.

1. Isolated follicle-stimulating hormone (FSH) deficiency in two infertile men without FSH β gene mutation: Case report and literature review

2. Hypogonadism Caused by a Single Amino Acid Substitution in the β Subunit of Luteinizing Hormone

3. Hypogonadism in a Patient with Two Novel Mutations of the Luteinizing Hormone β-Subunit Gene Expressed in a Compound Heterozygous Form

4. Initially Elevated TSH and Congenital Central Hypothyroidism Due to a Homozygous Mutation of the TSH Beta Subunit Gene: Case Report and Review of the Literature

5. GENETICS IN ENDOCRINOLOGY: Genetic counseling for congenital hypogonadotropic hypogonadism and Kallmann syndrome: new challenges in the era of oligogenism and next-generation sequencing