Atelosteogenesis type I

Editor-In-Chief: Prab R Tumpati, MD
Obesity, Sleep & Internal medicine
Founder, WikiMD Wellnesspedia &
W8MD medical weight loss NYC and sleep center NYC

Atelosteogenesis type I
Synonyms	AO type I
Pronounce	N/A
Specialty	N/A
Symptoms	Severe skeletal dysplasia, short limbs, joint dislocations, cleft palate, clubfoot
Complications	Respiratory failure, early death
Onset	Prenatal
Duration	Lifelong
Types	N/A
Causes	Mutations in the FLNB gene
Risks	Family history
Diagnosis	Prenatal ultrasound, genetic testing
Differential diagnosis	Atelosteogenesis type II, Diastrophic dysplasia, Achondrogenesis
Prevention	N/A
Treatment	Supportive care, palliative care
Medication	N/A
Prognosis	Poor, often lethal in infancy
Frequency	Rare
Deaths	N/A

Atelosteogenesis Type I

Diagram of autosomal dominant inheritance pattern

Atelosteogenesis Type I is a rare genetic disorder characterized by skeletal abnormalities. It is one of the types of atelosteogenesis, which are a group of disorders that affect bone development. Atelosteogenesis Type I is inherited in an autosomal dominant pattern, meaning that only one copy of the altered gene is sufficient to cause the disorder.

Clinical Features

Individuals with Atelosteogenesis Type I typically present with severe skeletal dysplasia. The clinical features include:

• Short limbs (rhizomelic shortening)
• Narrow chest
• Abnormalities of the spine
• Cleft palate
• Clubfoot

These features are usually apparent at birth or during prenatal ultrasound examinations.

Genetic Basis

Atelosteogenesis Type I is caused by mutations in the FLNB gene, which provides instructions for making a protein called filamin B. This protein is involved in the development and maintenance of the cytoskeleton, which is the structural framework that helps cells maintain their shape and internal organization.

Diagnosis

Diagnosis of Atelosteogenesis Type I is based on clinical evaluation, radiographic findings, and genetic testing. Prenatal diagnosis may be possible through ultrasound and genetic testing if there is a known family history of the disorder.

Management

There is no cure for Atelosteogenesis Type I, and management is primarily supportive. Treatment may involve:

• Orthopedic surgery to address skeletal abnormalities
• Respiratory support due to chest abnormalities
• Physical therapy to improve mobility

Prognosis

The prognosis for individuals with Atelosteogenesis Type I is generally poor. Many affected individuals do not survive past infancy due to respiratory complications. However, the severity of the condition can vary, and some individuals may live longer with appropriate medical care.

See also

• Skeletal dysplasia
• Autosomal dominant disorder
• Genetic testing