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What is Johnson-Hall-Krous syndrome?

What is Johnson-Hall-Krous syndrome?

  • Johnson-Hall-Krous syndrome: A rare congenital disorder characterized by cataracts, cleft palate, high nose bridge, extra finger and tongue abnormalities.

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

Johnson-Hall-Krous syndrome: Introduction

Types of Johnson-Hall-Krous syndrome:

Broader types of Johnson-Hall-Krous syndrome:

How serious is Johnson-Hall-Krous syndrome?

Prognosis of Johnson-Hall-Krous syndrome: Generally patients can expect a good prognosis.

What causes Johnson-Hall-Krous syndrome?

Causes of Johnson-Hall-Krous syndrome: see causes of Johnson-Hall-Krous syndrome

What are the symptoms of Johnson-Hall-Krous syndrome?

Symptoms of Johnson-Hall-Krous syndrome: see symptoms of Johnson-Hall-Krous syndrome

Johnson-Hall-Krous syndrome: Testing

Diagnostic testing: see tests for Johnson-Hall-Krous syndrome.

Misdiagnosis: see misdiagnosis and Johnson-Hall-Krous syndrome.

How is it treated?

Doctors and Medical Specialists for Johnson-Hall-Krous syndrome: Neonatologist ; see also doctors and medical specialists for Johnson-Hall-Krous syndrome.
Treatments for Johnson-Hall-Krous syndrome: see treatments for Johnson-Hall-Krous syndrome

Name and Aliases of Johnson-Hall-Krous syndrome

Main name of condition: Johnson-Hall-Krous syndrome

Other names or spellings for Johnson-Hall-Krous syndrome:

high nasal bridge, cataract and cleft palate, glossopalatine ankylosis [cataracts - digital anomalies], Glossopalatine ankylosis cataracts digital anomalies, Ankyloglossum Superius Syndrome, Oromandibular [Limb Hypogenesis Syndrome, Type III A], Oromandibular and Limb Hypogenesis Syndrome, Type III A, Cosack Syndrome


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