Aase syndrome
Aase-Smith syndrome

Most cases of Aase syndrome occur without a known reason and are not passed down through families (inherited).

Severe cases of Aase syndrome have been associated with stillbirth.

However, most cases of Aase syndrome are not inheritable.

Prednisone has also been used to treat anemia associated with Aase syndrome.

The exact cause of Aase syndrome is unknown.

Learn about causes, symptoms and treatments of Aase Syndrome.

Aase syndrome is thought to be an autosomal recessive inherited disorder.

The anemia in Aase syndrome is caused by poor development of the bone marrow, which is where blood cells are formed.

Aase syndrome is a rare disorder that involves anemia and certain joint and skeletal deformities.

Aase Syndrome Aase Syndrome information from HowStuffWorks.

Aase-Smith Syndrome II Congenital Anemia and Triphalangeal Thumbs Hypoplastic Anemia-Triphalangeal Thumbs, Aase-Smith Type None Aase syndrome is a rare genetic disorder that may be detected during early infancy.

Aase syndrome or Aase-Smith syndrome is a rare inherited disorder characterized by anemia with some joint and skeletal deformities.

Aase-Smith syndromes are deformities occurring in males characterised by a decreased production (hypoplasia) of red blood cells leading to anemia as well as certain joint contractures.

Aase-Smith Syndrome II Congenital Anemia and Triphalangeal Thumbs Hypoplastic Anemia-Triphalangeal Thumbs, Aase-Smith Type None Aase syndrome is a rare genetic disorder that may be detected during early infancy.