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Aase-Smith I syndrome

Aase-Smith I syndrome: Introduction

Aase-Smith I syndrome: A very rare hereditary syndrome characterized by deformities such as joint contractures, anemia, hydrocephalus and cleft palate. More detailed information about the symptoms, causes, and treatments of Aase-Smith I syndrome is available below.

Symptoms of Aase-Smith I syndrome

Home Diagnostic Testing

Home medical testing related to Aase-Smith I syndrome:

Wrongly Diagnosed with Aase-Smith I syndrome?

Aase-Smith I syndrome: Complications

Review possible medical complications related to Aase-Smith I syndrome:

Causes of Aase-Smith I syndrome

More information about causes of Aase-Smith I syndrome:

Aase-Smith I syndrome: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Aase-Smith I syndrome

Unnecessary hysterectomies due to undiagnosed bleeding disorder in women: The bleeding disorder called Von Willebrand's disease is quite common in women, but often fails to be correctly diagnosed. Women with the more »

Psoriatic arthritis often undiagnosed cause of joint conditions: Patients with the skin condition psoriasis can also have the related arthritis subtype called "psoriatic arthritis". This arthritic condition tends to be overlooked, more »

Aase-Smith I syndrome: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Aase-Smith I syndrome: Animations

Prognosis for Aase-Smith I syndrome

Prognosis for Aase-Smith I syndrome: Death usually occurs before birth or during infancy.

Statistics for Aase-Smith I syndrome

Aase-Smith I syndrome: Broader Related Topics

User Interactive Forums

Read about other experiences, ask a question about Aase-Smith I syndrome, or answer someone else's question, on our message boards:

Definitions of Aase-Smith I syndrome:

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Aase-Smith I syndrome as a "rare disease".
Source - Orphanet


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