{"database":"biostudies-literature","file_versions":[],"scores":null,"additional":{"omics_type":["Unknown"],"volume":["22(4)"],"submitter":["Chauhan P"],"pubmed_abstract":["<h4>Background</h4>Inhibin and activin regulate the follicle stimulating hormone level by their antagonistic actions and thus have been considered as strong candidate genes in the etiology of ovarian dysgenesis. In the present study, two cases of primary amenorrhea with poorly developed secondary sexual characteristics were reported. The purpose of the study was to identify mutations in candidate gene.<h4>Case presentation</h4>In this paper, clinical, genetic, biochemical, and molecular findings in female patients with primary amenorrhea were reported. Whole blood culture and G-banding for karyotyping, sequencing, and in silico analysis were performed following the standard protocol. Both cases were cytogenetically characterized as normal females with 46,XX, chromosome constitution. Hormon"],"journal":["Journal of reproduction & infertility"],"pagination":["295-301"],"full_dataset_link":["https://www.ebi.ac.uk/biostudies/studies/S-EPMC8669408"],"repository":["biostudies-literature"],"pubmed_title":["Identification of Novel Nucleotide Changes in INHBB Gene by Mutation Screening in Females with Ovarian Dysgenesis: A Case Report."],"pmcid":["PMC8669408"],"pubmed_authors":["Chauhan P","Rai AK","Rani A"],"additional_accession":[]},"is_claimable":false,"name":"Identification of Novel Nucleotide Changes in INHBB Gene by Mutation Screening in Females with Ovarian Dysgenesis: A Case Report.","description":"<h4>Background</h4>Inhibin and activin regulate the follicle stimulating hormone level by their antagonistic actions and thus have been considered as strong candidate genes in the etiology of ovarian dysgenesis. In the present study, two cases of primary amenorrhea with poorly developed secondary sexual characteristics were reported. The purpose of the study was to identify mutations in candidate gene.<h4>Case presentation</h4>In this paper, clinical, genetic, biochemical, and molecular findings in female patients with primary amenorrhea were reported. Whole blood culture and G-banding for karyotyping, sequencing, and in silico analysis were performed following the standard protocol. Both cases were cytogenetically characterized as normal females with 46,XX, chromosome constitution. Hormon","dates":{"release":"2021-01-01T00:00:00Z","publication":"2021 Oct-Dec","modification":"2025-04-03T22:45:56.5Z","creation":"2022-02-11T14:59:32.269Z"},"accession":"S-EPMC8669408","cross_references":{"pubmed":["34987992"],"doi":["10.18502/jri.v22i4.7656"]}}