Human genome variation, 2022-06, Vol.9 (1), p.23-23, Article 23
2022
Details
- Autor(en) / Beteiligte
- Titel
- Precocious puberty in a case of Simpson-Golabi-Behmel syndrome with a de novo 240-kb deletion including GPC3
- Ist Teil von
- Human genome variation, 2022-06, Vol.9 (1), p.23-23, Article 23
- Ort / Verlag
- England: Springer Nature B.V
- Erscheinungsjahr
- 2022
- Link zum Volltext
- Quelle
- Free E-Journal (出版社公開部分のみ）
- Beschreibungen/Notizen
- Here, we report a Japanese patient with Simpson-Golabi-Behmel syndrome involving a de novo 240-kb deletion including a part of GPC3. The patient showed pre- and postnatal macrosomia associated with coarse face, macrocephaly, supernumerary nipples, and cryptorchidism and characteristically presented with precocious puberty, mostly evaluated as advanced pubertal age of 15 years at the chronological age of 11.5 years.
- Sprache
- Englisch
- Identifikatoren
- ISSN: 2054-345XeISSN: 2054-345XDOI: 10.1038/s41439-022-00196-8Titel-ID: cdi_doaj_primary_oai_doaj_org_article_2478bc38e82348b7ac4fba166b10fc71
- Format
- –
- Schlagworte
- Cryptorchidism, Data Report, Genomes, Gestational age, Height, Heparan sulfate, Macrocephaly, Medicine, Mutation, Nipples, Parents & parenting, Patients, Pediatrics, Physical growth, Puberty, Supernumerary