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New disease
Accelerated coronary atherosclerosis and H syndrome
  1. Ravindranath K Shankarappa1,
  2. Rajiv Ananthakrishna1,
  3. Ravi S Math1,
  4. Sachin Dhareppa Yalagudri1,
  5. Satish Karur1,
  6. Ramesh Dwarakaprasad1,
  7. Manjunath C Nanjappa1,
  8. Vered Molho-Pessach2
  1. 1Cardiology Department, Sri Jayadeva Institute of Cardiovascular Sciences and Research, Bangalore, Karnataka, India
  2. 2Dermatology Department and Center for Genetic Diseases of the Skin and Hair, Hadassah-Hebrew University Medical Center, Jerusalem, Israel
  1. Correspondence to Dr Rajiv Ananthakrishna, rajiva.ms{at}gmail.com

Summary

A 12-year-old boy with insulin dependent diabetes mellitus, presented with acute myocardial infarction. Intracoronary thrombolysis with urokinase restored TIMI III flow in the culprit vessel. After stabilisation with medical therapy, unusual clinical findings in the form of cutaneous hyperpigmentation and hypertrichosis, affecting the lower extremities, were appreciated. These and other phenotypic features were consistent with H syndrome, a recently described autosomal recessive genodermatosis, and confirmed by mutation analysis. Despite being on optimal medical therapy for coronary artery disease, the patient presented 3 months thereafter, with unstable angina which was successfully managed with percutaneous coronary intervention. An unusual occurrence of coronary artery disease with accelerated atherosclerosis in a child with H syndrome is presented herein. Identification of further patients with this novel disorder will clarify the possible association, suggested here, with increased risk for coronary or other vascular events.

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Footnotes

  • Competing interests None.

  • Patient consent Obtained.

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