Acromesomelic dysplasia
rareA group of extremely rare, inherited, progressive skeletal conditions that result in a particular form of short stature, called short-limb dwarfism. The short stature is the result of unusually short forearms and forelegs (mesomelia) and abnormal shortening of the bones in the hands and feet (acromelia). At birth, the hands and feet may appear abnormally short and broad. Over time, the apparent disproportion becomes even more obvious, especially during the first years of life. Additional features may include: limited extension of the elbows and arms; progressive abnormal curvature of the spine; an enlarged head; and a slightly flattened midface. Acromesomelic dysplasia is inherited as an autosomal recessive trait. There are different types of acromesomelic dysplasia, which are distinguished by their genetic cause. To read more about the different types, click on the links below. Acromesomelic dysplasia, Maroteaux type Acromesomelic dysplasia, Hunter-Thompson type Acromesomelic dysplasia, Grebe type
- Identifiers
- MONDO:0019696 Orphanet:93437
- Part of
- Osteochondrodysplasia
- Also known as
- acromesomelic dwarfism
Subtypes
- Osebold-Remondini syndrome MONDO:0007219
- Acromesomelic dysplasia 1, Maroteaux type MONDO:0011275 NPR2
- Acromesomelic dysplasia 2A MONDO:0008703 GDF5
- Acromesomelic dysplasia 2B MONDO:0009231 GDF5
- Acromesomelic dysplasia 2C, Hunter-Thompson type MONDO:0008717 GDF5
- Acromesomelic dysplasia 3 MONDO:0012274 BMPR1B
- Acromesomelic dysplasia 4 MONDO:0030553 PRKG2
- Acromesomelic dysplasia, Campailla Martinelli type MONDO:0021805
Projects
Including projects on subtypes.
No projects yet.