Conditions / Syndrome
dilated cardiomyopathy-hypergonadotropic hypogonadism syndrome
info · Syndrome
A syndrome characterized by dilated cardiomyopathy and hypergonadotropic hypogonadism that has_material_basis_in heterozygous mutation in the LMNA gene on chromosome 1q22.
Signs and symptoms
- Poor wound healing
- Short chin
- Narrow nose
- Sclerodactyly
- Recurrent shoulder dislocation
- Telangiectasia of the skin
- Finger joint contracture
- Microtia
- Cardiomyopathy
- Mitral regurgitation
Also known as: Malouf syndrome; Najjar syndrome; cardiogenital syndrome; cardiomyopathy eith primary testicular failure; congestive cardiomyopathy with hypergonadotropic hypogonadism