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...

Täydet tiedot

Bibliografiset tiedot
Päätekijät: Erika Nakajima, Yuko Yokohama, Saori Sugiyama, Mio Taketazu, Kenrokuro Mitsube, Takahiro Yamada, Anna Hammarsjö, Giedre Grigelioniene, Gen Nishimura, Yoshio Makita
Aineistotyyppi: Artikkeli
Kieli:English
Julkaistu: Nature Publishing Group 2024-12-01
Sarja:Human Genome Variation
Linkit:https://doi.org/10.1038/s41439-024-00302-y