| Literature DB >> 27071470 |
Julianna E Shinnick1, Kimberly Schadt1, Cassandra Strawser1, Nicholas Wilcox1, Susan L Perlman2, George R Wilmot3, Christopher M Gomez4, Katherine D Mathews5, Grace Yoon6, Theresa Zesiewicz7, Chad Hoyle8, S H Subramony9, Eppie M Yiu10, Martin B Delatycki10, Alicia F Brocht11, Jennifer M Farmer1, David R Lynch12.
Abstract
Friedreich ataxia is a progressive degenerative disease with neurologic and cardiac involvement. This study characterizes comorbid medical conditions in a large cohort of patients with Friedreich ataxia. Patient diagnoses were collected in a large natural history study of 641 subjects. Prevalence of diagnoses in the cohort with Friedreich ataxia was compared with prevalence in the population without Friedreich ataxia. Ten patients (1.6%) had inflammatory bowel disease, 3.5 times more common in this cohort of individuals with Friedreich ataxia than in the general population. Four subjects were growth hormone deficient, reflecting a prevalence in Friedreich ataxia that is 28 times greater than the general population. The present study identifies specific diagnoses not traditionally associated with Friedreich ataxia that are found at higher frequency in this disease. These associations could represent coincidence, shared genetic background, or potentially interactive disease mechanisms with Friedreich ataxia.Entities:
Keywords: Friedreich ataxia; comorbidity; growth hormone deficiency; inflammatory bowel disease
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Year: 2016 PMID: 27071470 DOI: 10.1177/0883073816643408
Source DB: PubMed Journal: J Child Neurol ISSN: 0883-0738 Impact factor: 1.987