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What is Megarbane-Jalkh Syndrome?

What is Megarbane-Jalkh Syndrome?

  • Megarbane-Jalkh Syndrome: A rare condition reported in two related infants and involving a range of abnormalities such as developmental delay, unusual facial features, wrinkled skin, liver failure and fragile bones. One of the infants died before the age of 2 years due to liver failure.

Megarbane-Jalkh Syndrome: Introduction

Types of Megarbane-Jalkh Syndrome:

Broader types of Megarbane-Jalkh Syndrome:

How serious is Megarbane-Jalkh Syndrome?

Complications of Megarbane-Jalkh Syndrome: see complications of Megarbane-Jalkh Syndrome

What causes Megarbane-Jalkh Syndrome?

Causes of Megarbane-Jalkh Syndrome: see causes of Megarbane-Jalkh Syndrome

What are the symptoms of Megarbane-Jalkh Syndrome?

Symptoms of Megarbane-Jalkh Syndrome: see symptoms of Megarbane-Jalkh Syndrome

Complications of Megarbane-Jalkh Syndrome: see complications of Megarbane-Jalkh Syndrome

Megarbane-Jalkh Syndrome: Testing

Diagnostic testing: see tests for Megarbane-Jalkh Syndrome.

Misdiagnosis: see misdiagnosis and Megarbane-Jalkh Syndrome.

How is it treated?

Treatments for Megarbane-Jalkh Syndrome: see treatments for Megarbane-Jalkh Syndrome

Name and Aliases of Megarbane-Jalkh Syndrome

Main name of condition: Megarbane-Jalkh Syndrome

Other names or spellings for Megarbane-Jalkh Syndrome:

Developmental Delay, Dysmorphic Features, Neonatal Spontaneous Fractures, Wrinkled Skin and Hepatic Failure

 

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