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What is Camptodactyly -- joint contractures and facial skeletal dysplasia?

What is Camptodactyly -- joint contractures and facial skeletal dysplasia?

  • Camptodactyly -- joint contractures and facial skeletal dysplasia: A rare genetic disorder characterized by joint contractures, drooping eyelids, spinal curvature and permanently bent fingers (camptodactyly).

Camptodactyly -- joint contractures and facial skeletal dysplasia is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Camptodactyly -- joint contractures and facial skeletal dysplasia, or a subtype of Camptodactyly -- joint contractures and facial skeletal dysplasia, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

Camptodactyly -- joint contractures and facial skeletal dysplasia: Introduction

Types of Camptodactyly -- joint contractures and facial skeletal dysplasia:

Broader types of Camptodactyly -- joint contractures and facial skeletal dysplasia:

What causes Camptodactyly -- joint contractures and facial skeletal dysplasia?

Causes of Camptodactyly -- joint contractures and facial skeletal dysplasia: see causes of Camptodactyly -- joint contractures and facial skeletal dysplasia

What are the symptoms of Camptodactyly -- joint contractures and facial skeletal dysplasia?

Symptoms of Camptodactyly -- joint contractures and facial skeletal dysplasia: see symptoms of Camptodactyly -- joint contractures and facial skeletal dysplasia

Camptodactyly -- joint contractures and facial skeletal dysplasia: Testing

Misdiagnosis: see misdiagnosis and Camptodactyly -- joint contractures and facial skeletal dysplasia.

How is it treated?

Doctors and Medical Specialists for Camptodactyly -- joint contractures and facial skeletal dysplasia: Orthopedic surgeon ; see also doctors and medical specialists for Camptodactyly -- joint contractures and facial skeletal dysplasia.
Treatments for Camptodactyly -- joint contractures and facial skeletal dysplasia: see treatments for Camptodactyly -- joint contractures and facial skeletal dysplasia

Name and Aliases of Camptodactyly -- joint contractures and facial skeletal dysplasia

Main name of condition: Camptodactyly -- joint contractures and facial skeletal dysplasia

Other names or spellings for Camptodactyly -- joint contractures and facial skeletal dysplasia:

Rozin-Hertz-Goodman syndrome, Joint contractures, right acetabular dysplasia, ulno-fibular dysostosis, and bilateral talipes equinovarus with calcaneocuboid fusion, Camptodactyly, joint contractures, facial skeletal defects, Camptodactyly, myopia, and fibrosis of the medial rectus muscle of eye

Joint contractures, right acetabular 'dysplasia,' ulno-fibular dysostosis, and bilateral talipes equinovarus with calcaneocuboid fusion
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Camptodactyly -- joint contractures and facial skeletal dysplasia: Related Conditions

Research the causes of these diseases that are similar to, or related to, Camptodactyly -- joint contractures and facial skeletal dysplasia:

 

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