Ontology highlight
ABSTRACT:
SUBMITTER: Tomaselli PJ
PROVIDER: S-EPMC6302219 | biostudies-literature | 2018 Dec
REPOSITORIES: biostudies-literature
Tomaselli Pedro J PJ Horga Alejandro A Rossor Alexander M AM Jaunmuktane Zane Z Cortese Andrea A Blake Julian C JC Zarate-Lopez Natalia N Houlden Henry H Reilly Mary M MM
Neuromuscular disorders : NMD 20180829 12
Biallelic mutations in the IGHMBP2 have been associated with two distinct phenotypes: spinal muscular atrophy with respiratory distress type 1 (SMARD1) and CMT2S. We describe a patient who developed progressive muscle weakness and wasting in her upper and lower limbs from infancy. She developed respiratory involvement at age 9, eventually requiring 24-h non-invasive ventilation, and severe autonomic dysfunction restricted to the gastrointestinal tract. Neurophysiological studies at age 27 years ...[more]