Unclassifiable short-rib thoracic dysplasia diagnosed using targeted gene panel sequencing
Abstract We report a case of a fetus with short-rib thoracic dysplasia (SRTD) with polydactyly that also presented with atypical severe acro-mesomelic ossification defects. Genetic analysis using massively parallel sequencing of a skeletal dysplasia panel revealed compound heterozygous variants in D...
المؤلفون الرئيسيون: | Erika Nakajima, Yuko Yokohama, Saori Sugiyama, Mio Taketazu, Kenrokuro Mitsube, Takahiro Yamada, Anna Hammarsjö, Giedre Grigelioniene, Gen Nishimura, Yoshio Makita |
---|---|
التنسيق: | مقال |
اللغة: | English |
منشور في: |
Nature Publishing Group
2024-12-01
|
سلاسل: | Human Genome Variation |
الوصول للمادة أونلاين: | https://doi.org/10.1038/s41439-024-00302-y |
مواد مشابهة
-
Exploring human genetic skeletal disorders provides important insights into skeletogenesis and elucidates basic developmental signaling pathways
حسب: Giedre Grigelioniene, وآخرون
منشور في: (2020-12-01) -
Case Report: Inversion of LMX1B - A Novel Cause of Nail-Patella Syndrome in a Swedish Family and a Longtime Follow-Up
حسب: Hillevi Lindelöf, وآخرون
منشور في: (2022-06-01) -
Case report: Extending the spectrum of clinical and molecular findings in FOXC1 haploinsufficiency syndrome
حسب: Alexandra Garza Flores, وآخرون
منشور في: (2023-06-01) -
Patient with unclassifiable rhinophyma
حسب: Cocepción Isabel Pereira Dávalos, وآخرون
منشور في: (2021-12-01) -
Severe and unclassifiable tremor
حسب: Marcos Serrano-Dueñas
منشور في: (2024-10-01)