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  3. Research By Disease

Disease: Cardiomyopathy hypogonadism metabolic anomalies

  • Alström Syndrome
  • Case of ovarian dysgenesis and dilated cardiomyopathy supports existence of Malouf syndrome
  • Comprehensive Endocrine-Metabolic Evaluation of Patients With Alstrom Syndrome Compared With BMI-Matched Controls
  • Coronary artery disease in Alström syndrome
  • Differences in the clinical spectrum of two adolescent male patients with Alström syndrome
  • Endocrine abnormalities in mitochondrial myopathy with external ophthalmoplegia
  • Endocrine dysfunction in Kearns-Sayre syndrome
  • Familial variable expression of dilated cardiomyopathy in Alstrom syndrome: a report of four sibs
  • Inherited hemochromatosis: from genetics to clinics
  • ITPase deficiency causes a Martsolf-like syndrome with a lethal infantile dilated cardiomyopathy
  • Late onset dilated cardiomyopathy in a unique familial syndrome of hypogonadism and metabolic abnormalities
  • Management of hemochromatosis. Hemochromatosis Management Working Group
  • Medical treatment of acromegaly: comorbidities and their reversibility by somatostatin analogs
  • The Alström syndrome: is it a rare or unknown disease?
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CheckOrphan is a non-profit organization located in Basel, Switzerland and Santa Cruz, California that is dedicated to rare, orphan and neglected diseases. CheckOrphan offers users an interactive and dynamic platform for all these diseases. This strategy allows visitors to be updated daily on all the latest news and interact with people internationally. This is essential, because due to the nature of these diseases, there is not a large concentration of individuals within any given proximity.
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