SF1 and spleen development: new heterozygous mutation, literature review and consequences for NR5A1- mutated patient's management

التفاصيل البيبلوغرافية
العنوان: SF1 and spleen development: new heterozygous mutation, literature review and consequences for NR5A1- mutated patient's management
المؤلفون: Maryse Cartigny, Cindy Colson, Estelle Aubry, Rémi Besson, Xavier Leroy, Anne-Françoise Spinoit, Sylvie Manouvrier, Jamal Ghoumid, Pascal Philibert, Helene Franquet, Charles Sultan, Martine Cools, Amélie‐Anne Rémy, Géraldine Kéchid, Christine Lefèvre
المصدر: Clinical Genetics. 92:99-103
بيانات النشر: Wiley, 2017.
سنة النشر: 2017
مصطلحات موضوعية: 0301 basic medicine, Steroidogenic factor 1, Proband, Genetics, endocrine system, Mutation, Asplenia, 030209 endocrinology & metabolism, Sex reversal, Biology, medicine.disease, medicine.disease_cause, 3. Good health, Premature ovarian failure, 03 medical and health sciences, 030104 developmental biology, 0302 clinical medicine, medicine, Polysplenia, Adrenocortical Insufficiency, Genetics (clinical)
الوصف: Steroidogenic factor 1 (encoded by SF1/NR5A1) is a transcription factor with multiple target genes involved in the development and function of multiple steroidogenic and non-steroidogenic tissues. NR5A1 mutations lead to several phenotypes, including sex reversal, spermatogenesis failure, premature ovarian failure and adrenocortical insufficiency. The implication of NR5A1 mutations in spleen development anomalies was recently highlighted. We provide new evidence of this involvement, describing a novel heterozygous non-sense NR5A1 mutation in a 46,XY-DSD with polysplenia female proband and her father, who had hypospadias and asplenia.
تدمد: 0009-9163
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_________::da4fc7d66a19f908946618f006275560Test
https://doi.org/10.1111/cge.12957Test
حقوق: CLOSED
رقم الانضمام: edsair.doi...........da4fc7d66a19f908946618f006275560
قاعدة البيانات: OpenAIRE