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What is Catel-Manzke Syndrome?

What is Catel-Manzke Syndrome?

  • Catel-Manzke Syndrome: A rare genetic disorder characterized by a small jaw, cleft palate and an extra bone at the base of the pointer finger.

Catel-Manzke Syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Catel-Manzke Syndrome, or a subtype of Catel-Manzke Syndrome, affects less than 200,000 people in the US population.
Source - National Institutes of Health (NIH)

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

Catel-Manzke Syndrome: Introduction

Types of Catel-Manzke Syndrome:

Broader types of Catel-Manzke Syndrome:

How serious is Catel-Manzke Syndrome?

Complications of Catel-Manzke Syndrome: see complications of Catel-Manzke Syndrome

What causes Catel-Manzke Syndrome?

Causes of Catel-Manzke Syndrome: see causes of Catel-Manzke Syndrome
Risk factors for Catel-Manzke Syndrome: see risk factors for Catel-Manzke Syndrome

What are the symptoms of Catel-Manzke Syndrome?

Symptoms of Catel-Manzke Syndrome: see symptoms of Catel-Manzke Syndrome

Complications of Catel-Manzke Syndrome: see complications of Catel-Manzke Syndrome

Catel-Manzke Syndrome: Testing

Diagnostic testing: see tests for Catel-Manzke Syndrome.

Misdiagnosis: see misdiagnosis and Catel-Manzke Syndrome.

How is it treated?

Doctors and Medical Specialists for Catel-Manzke Syndrome: Medical Geneticist ; see also doctors and medical specialists for Catel-Manzke Syndrome.
Treatments for Catel-Manzke Syndrome: see treatments for Catel-Manzke Syndrome
Research for Catel-Manzke Syndrome: see research for Catel-Manzke Syndrome

Name and Aliases of Catel-Manzke Syndrome

Main name of condition: Catel-Manzke Syndrome

Other names or spellings for Catel-Manzke Syndrome:

Hyperphalangy-clinodactyly of index finger with Pierre Robin syndrome, Pierre Robin syndrome with hyperphalangy and clinodactyly, Palatodigital syndrome, Catel-Manzke type, Pierre robin syndrome [hyperphalangy - clinodactyly], Oromandibular [Limb Hypogenesis Syndrome, Type V C], Oromandibular and Limb Hypogenesis Syndrome, Type V C

Hyperphalangy-clinodactyly of index finger with Pierre Robin syndrome, Palatodigital syndrome, Catel-Manzke type, Pierre Robin syndrome with hyperphalangy and clinodactyly
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

Catel-Manzke Syndrome: Related Conditions

Research the causes of these diseases that are similar to, or related to, Catel-Manzke Syndrome:

 

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