Noncompaction of the myocardium associated with Roifman syndrome.

Abstract

Noncompaction of the ventricular myocardium, sometimes referred to as "spongy myocardium", appears as excessive and prominent trabeculations and deep intratrabecular recesses within the ventricular wall, usually involving the left ventricle, although the right ventricle and interventricular septum can also be affected. It may occur with or without additional heart malformations. Roifman syndrome is a constellation of antibody deficiency, spondyloepiphyseal dysplasia, facial dysmorphism, growth retardation, and retinal dystrophy. We report a patient with Roifman syndrome who presented with noncompaction of the left ventricular myocardium. Our findings expand the spectrum of diseases associated with noncompaction. The recognition of noncompaction among patients with Roifman syndrome is important, as the immune deficiencies may be subtle and undiagnosed until adulthood. Thus, some patients may first present with cardiac failure.

• Authors: K Mandel, E Grunebaum, L Benson
• Journal: Cardiology in the young (Cardiol Young) Vol. 11 Issue 2 Pg. 240-3 (Mar 2001) ISSN: 1047-9511 [Print] England
• PMID: 11293748 (Publication Type: Case Reports, Journal Article)

Topics

• Adolescent
• Bone Diseases, Developmental (genetics, pathology)
• Cardiomyopathies (genetics, pathology)
• Humans
• Immunologic Deficiency Syndromes (genetics, pathology)
• Male
• Syndrome
• X Chromosome