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What is Teebi-Kaurah syndrome?

What is Teebi-Kaurah syndrome?

  • Teebi-Kaurah syndrome: A very rare syndrome characterized mainly by a small head and absent nails.

Teebi-Kaurah syndrome is listed as a "rare disease" by the Office of Rare Diseases (ORD) of the National Institutes of Health (NIH). This means that Teebi-Kaurah syndrome, or a subtype of Teebi-Kaurah 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 Teebi-Kaurah syndrome as a "rare disease".
Source - Orphanet

Teebi-Kaurah syndrome: Introduction

Types of Teebi-Kaurah syndrome:

Broader types of Teebi-Kaurah syndrome:

What causes Teebi-Kaurah syndrome?

Causes of Teebi-Kaurah syndrome: see causes of Teebi-Kaurah syndrome

What are the symptoms of Teebi-Kaurah syndrome?

Symptoms of Teebi-Kaurah syndrome: see symptoms of Teebi-Kaurah syndrome

Teebi-Kaurah syndrome: Testing

Misdiagnosis: see misdiagnosis and Teebi-Kaurah syndrome.

How is it treated?

Doctors and Medical Specialists for Teebi-Kaurah syndrome: Neonatologist, Neurologist ; see also doctors and medical specialists for Teebi-Kaurah syndrome.
Treatments for Teebi-Kaurah syndrome: see treatments for Teebi-Kaurah syndrome

Name and Aliases of Teebi-Kaurah syndrome

Main name of condition: Teebi-Kaurah syndrome

Other names or spellings for Teebi-Kaurah syndrome:

anonychia [microcephaly], Total anonychia congenita and microcephaly with normal intelligence

Total anonychia congenita and microcephaly with normal intelligence
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)


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