Mulibrey nanism ("MUscle-LIver-BRain-EYe nanism"), also called Perheentupa syndrome and pericardial constriction with growth failure,  is a rare autosomal ...
Summarizes the state of knowledge of mulibrey nanism, also known as Perheentupa Syndrome.
Important It is possible that the main title of the report Mulibrey Nanism Syndrome (Perheentupa Syndrome) is not the name you expected. Please check the ...
Mulibrey nanism is a rare genetic disorder characterized by profound growth delays and distinctive abnormalities of the muscles, liver, brain, and eyes.
Mulibrey nanism is an extremely rare autosomal recessive genetic disorder characterized by profound growth delays and distinctive abnormalities of the muscles, liver ...
General Discussion. Mulibrey nanism is an extremely rare autosomal recessive genetic disorder characterized by profound growth delays and distinctive abnormalities of ...
Mulibrey Nanism syndrome information including symptoms, diagnosis, misdiagnosis, treatment, causes, patient stories, videos, forums, prevention, and prognosis.
Perheentupa J, Autio S, Leisti S, Raitta C, Tuuteri L. Mulibrey nanism, an autosomal recessive syndrome with pericardial constriction. Lancet.
Summary. MULIBREY nanism (MUL) is a prenatal onset growth disorder with multiorgan manifestations. The exact prevalence is unknown, though 115 cases have been ...
mu·li·brey nan·ism (mŭ'li-brā), [MIM*253250] Because mulibrey is not a proper noun, it is spelled with a lowercase m. autosomal recessive disorder with defects ...