Mulibrey Nanism Overview

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Learn About Mulibrey Nanism

What is the definition of Mulibrey Nanism?
Mulibrey Nanism is a rare genetic disorder characterized by profound growth delays and distinctive abnormalities of the muscles, liver, brain, and eyes. The acronym MULIBREY stands for (MU)scle, (LI)ver, (BR)ain, and (EY)e; nanism is another word for dwarfism. Signs and symptoms of the disorder may include constrictive pericarditis; low birth weight; short stature; severe progressive growth delays; hypotonia; hepatomegaly; and yellow discoloration of the eyes in infancy. It is caused by genetic changes in the TRIM37 gene and is inherited in an autosomal recessive manner.
What are the alternative names for Mulibrey Nanism?
  • Mulibrey Nanism
  • Muscle-liver-brain-eye nanism
  • Perheentupa syndrome
  • Pericardial constriction and growth failure
Who are the top Mulibrey Nanism Local Doctors?
Elite in Mulibrey Nanism
Marita Nyman-Lipsanen
Elite in Mulibrey Nanism
Marita Nyman-Lipsanen
Helsinki, FI 

Marita Nyman-Lipsanen practices in Helsinki, Finland. Ms. Nyman-Lipsanen is rated as an Elite expert by MediFind in the treatment of Mulibrey Nanism. Her top areas of expertise are Mulibrey Nanism, Genital Dwarfism, Russell-Silver Dwarfism, and Isolated ACTH Deficiency.

Elite in Mulibrey Nanism
Hannu J. Jalanko
Elite in Mulibrey Nanism
Hannu J. Jalanko
Pl 347, 
Helsinki, FI 

Hannu Jalanko practices in Helsinki, Finland. Jalanko is rated as an Elite expert by MediFind in the treatment of Mulibrey Nanism. Their top areas of expertise are Mulibrey Nanism, Biliary Atresia, Congenital Nephrotic Syndrome, Kidney Transplant, and Liver Transplant.

 
 
 
 
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Elite in Mulibrey Nanism
Riitta Karikoski
Elite in Mulibrey Nanism
Riitta Karikoski
Helsinki, FI 

Riitta Karikoski practices in Helsinki, Finland. Karikoski is rated as an Elite expert by MediFind in the treatment of Mulibrey Nanism. Their top areas of expertise are Mulibrey Nanism, Genital Dwarfism, Enlarged Liver, and Cardiomyopathy.

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Published Date: May 02, 2022
Published By: Genetic and Rare Diseases Informnation Center