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...
Main Authors: | Erika Nakajima, Yuko Yokohama, Saori Sugiyama, Mio Taketazu, Kenrokuro Mitsube, Takahiro Yamada, Anna Hammarsjö, Giedre Grigelioniene, Gen Nishimura, Yoshio Makita |
---|---|
Format: | Article |
Language: | English |
Published: |
Nature Publishing Group
2024-12-01
|
Series: | Human Genome Variation |
Online Access: | https://doi.org/10.1038/s41439-024-00302-y |
Similar Items
-
Exploring human genetic skeletal disorders provides important insights into skeletogenesis and elucidates basic developmental signaling pathways
by: Giedre Grigelioniene, et al.
Published: (2020-12-01) -
Case Report: Inversion of LMX1B - A Novel Cause of Nail-Patella Syndrome in a Swedish Family and a Longtime Follow-Up
by: Hillevi Lindelöf, et al.
Published: (2022-06-01) -
Case report: Extending the spectrum of clinical and molecular findings in FOXC1 haploinsufficiency syndrome
by: Alexandra Garza Flores, et al.
Published: (2023-06-01) -
Patient with unclassifiable rhinophyma
by: Cocepción Isabel Pereira Dávalos, et al.
Published: (2021-12-01) -
Severe and unclassifiable tremor
by: Marcos Serrano-Dueñas
Published: (2024-10-01)