Atelosteogenesis, type 2 |
AO2; De la Chapelle dysplasia; McAlister dysplasia; Neonatal osseous dysplasia 1 |
Atelosteogenesis, type 2 is a severe disorder of cartilage and bone development. Infants born with this condition have very short arms and legs, a narrow chest, and a prominent, rounded abdomen. This disorder is also characterized by an opening in the roof of the mouth (cleft palate), distinctive facial features, an inward- and downward-turning foot (clubfoot), and unusually positioned thumbs (hitchhiker thumbs). The signs and symptoms of atelosteogenesis, type 2 are similar to those of another skeletal disorder called diastrophic dysplasia. Atelosteogenesis, type 2 tends to be more severe, however. Infants with this disorder are usually stillborn or die shortly after birth from respiratory failure. Some affected infants have survived for a time with intensive medical support.
Atelosteogenesis, type II is a severe disorder of cartilage and bone develop ...
From the WEST scientific·clinical |
From the EAST traditional·alternative |
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Atelosteogenesis, type 2 Other1 of 1
Atelosteogenesis, type 2
... Atelosteogenesis, type 2 is a severe disorder of cartilage and bone development. Infants born with this condition have very short arms and legs, a narrow chest, and a prominent, rounded abdomen. This ...
Source: Genetics Home Reference
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Atelosteogenesis, type 2 Articles
- Atelosteogenesis, type 2
... Atelosteogenesis, type 2 is a severe disorder of cartilage and bone development. Infants born with this condition have very short arms and legs, a narrow chest, and a prominent, rounded abdomen. This ...

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