Lessons Learned from 17 Years of Multidisciplinary Care for DSD Patients at A Single Indonesian Center
CONCLUSIONS: Our work has highlighted the occurrence of different DSDs in Indonesia. By applying sequencing technologies as part of our clinical care, we have delivered a number of genetic diagnoses and identified novel pathogenic variants in some genes, which may be clinically specific to Indonesia. Genetics can inform many aspects of DSD clinical management, and whilst many of our patients remain undiagnosed, we hope that future testing may provide answers for even more.PMID:37699373 | DOI:10.1159/000534085
Source: Sexual Development : genetics, molecular biology, evolution, endocrinology, embryology, and pathology of sex determination and differentiation - Category: Genetics & Stem Cells Authors: Sultana Mh Faradz Nurin Listyasari Agustini Utari Mahayu Dewi Ariani Achmad Zulfa Juniarto Ardy Santosa Annastasia Ediati Tuula K Rinne Dineke Westra Hedi Claahsen-van der Grinten Frank H de Jong Stenvert Ls Drop Katie Ayers Andrew Sinclair Source Type: research
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