Congenital muscular dystrophy in a dog with a LAMA2 gene deletion.
G Diane SheltonKatie M MinorStephanie ThomovskyLing T GuoSteven G FriedenbergJonah N CullenJames R MickelsonPublished in: Journal of veterinary internal medicine (2021)
A 2-year-old female spayed dog was presented with a chronic history of short-strided gait and inability to completely open the jaw. Clinical signs were present since the dog was adopted from a humane society at a few months of age. Serum creatine kinase activity was abnormally high. Neurological examination, electromyography, muscle biopsies with immunofluorescent staining, and whole genome sequencing (WGS) were performed. A dystrophic phenotype was identified histologically in muscle biopsies, deficiency of laminin α2 protein was confirmed by immunofluorescent staining, and a deletion in the LAMA2 gene was identified by analysis of the WGS data. Congenital muscular dystrophy associated with a disease variant in LAMA2 was identified.
Keyphrases
- muscular dystrophy
- duchenne muscular dystrophy
- skeletal muscle
- copy number
- genome wide
- genome wide identification
- flow cytometry
- ultrasound guided
- electronic health record
- tyrosine kinase
- machine learning
- protein protein
- protein kinase
- gene expression
- deep learning
- small molecule
- artificial intelligence
- data analysis
- subarachnoid hemorrhage