Literature DB >> 23456527

Brachydactylia as a phenotypic feature of mitochondrial disorder.

Josef Finsterer1, Walte Strobl.   

Abstract

Mitochondrial disorders (MIDs) may occasionaly go along with dysmorphism but hand deformities, as in the following case, have been only rarely reported. A 72 year old female with ptosis, hypoacusis, tremor, myopathy, diabetes mellitus, arterial hypertension, severe cardiac disease, pulmonary hypertension, gastric carcinoid, hepatopathy, generalised atherosclerosis, anemia, polyarthrosis, and hyperlipidemia, additionally presented with brachydactylia. Upon neurological work-up a MID was suspected. The family history was positive for diabetes but negative for brachydactylia or other features of a MID. MIDs may be associated with brachydactylia. Skeletal deformities may be a phenotypic manifestation of MIDs.
© 2012 Tehran University of Medical Sciences. All rights reserved.

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Year:  2012        PMID: 23456527

Source DB:  PubMed          Journal:  Acta Med Iran        ISSN: 0044-6025


  2 in total

1.  Camptocormia and Other Orthopedic Compromise Dominating Mitochondrial Disorder: A Case Report.

Authors:  Josef Finsterer; Subhankar Chatterjee; Ritwik Ghosh
Journal:  Cureus       Date:  2020-12-03

2.  Mitochondrial Encephalomyopathy, Lactic Acidosis, and Stroke-Like Episodes (MELAS) in the 18th Century: Mitochondrial Disorders Are Not of Recent Origin.

Authors:  John Hayman; Steven Pavlakis; Josef Finsterer
Journal:  Cureus       Date:  2022-02-17
  2 in total

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