Open Directory - Health: Conditions and Diseases: Musculoskeletal Disorders: Congenital Anomalies: Dwarfism: Mulibrey Nanismtal Anomalies: Dwarfism: Mulibrey Nanism

Description

See also:

Mulibrey Nanism: Clinical Features and Diagnostic Criteria - Karlberg, Jalanko, Perheentupa and Lipsanen-Nyman review symptoms of 85 Finnish patients, and propose new diagnostic criteria for MUL. [PDF]
Online Inheritance in Man - Summarizes the state of knowledge of mulibrey nanism, also known as Perheentupa Syndrome.
Patient UK: Mulibrey Nanism - Factsheet on this rare autosomal recessive disorder, its clinical features, associated diseases and management.

"Mulibrey Nanism" search on: AOL - Ask - Bing - Gigablast - Google - Lycos - Yahoo - Yippy

Volunteer to edit this category.

Visit our sister sites mozilla.org | MusicMoz | Wikipedia

Last update: Tuesday, January 2, 2007 4:35:23 PM EST - edit

Open Directory - Health: Conditions and Diseases: Musculoskeletal Disorders: Congenital Anomalies: Dwarfism: Mulibrey Nanismtal Anomalies: Dwarfism: Mulibrey Nanism

about dmoz | help

Mulibrey nanism (MUscle-LIver-BRain-EYe nanism) is a rare growth disorder of prenatal onset caused by mutations in the TRIM37 gene. Mulibrey nanism is inherited autosomally recessively, and is characterized by prenatal-onset growth failure, constrictive cardiopathy, hepatomegaly, muscle hypotonia, J-shaped sella turcica, yellowish dots in the retinal midperiphery, and typical appearance.

Open Directory Health: Conditions and Diseases: Genetic Disorders
Open Directory Regional: Europe: Finland: Health: Conditions and Diseases

Last update: Tuesday, January 2, 2007 4:35:23 PM EST - edit

Help build the largest human-edited directory on the web.

Submit a Site - Open Directory Project - Become an Editor

About Serebella.com