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What is Jones-Hersh-Yusk syndrome?

What is Jones-Hersh-Yusk syndrome?

  • Jones-Hersh-Yusk syndrome: A rare congenital disorder characterized by missing toes, cleft palate, blistered skin and absent patches of skin at birth.

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

Jones-Hersh-Yusk syndrome: Introduction

Types of Jones-Hersh-Yusk syndrome:

Broader types of Jones-Hersh-Yusk syndrome:

What causes Jones-Hersh-Yusk syndrome?

Causes of Jones-Hersh-Yusk syndrome: see causes of Jones-Hersh-Yusk syndrome

What are the symptoms of Jones-Hersh-Yusk syndrome?

Symptoms of Jones-Hersh-Yusk syndrome: see symptoms of Jones-Hersh-Yusk syndrome

Jones-Hersh-Yusk syndrome: Testing

Misdiagnosis: see misdiagnosis and Jones-Hersh-Yusk syndrome.

How is it treated?

Doctors and Medical Specialists for Jones-Hersh-Yusk syndrome: Neonatologist, Craniofacial Surgeon ; see also doctors and medical specialists for Jones-Hersh-Yusk syndrome.
Treatments for Jones-Hersh-Yusk syndrome: see treatments for Jones-Hersh-Yusk syndrome

Name and Aliases of Jones-Hersh-Yusk syndrome

Main name of condition: Jones-Hersh-Yusk syndrome

Other names or spellings for Jones-Hersh-Yusk syndrome:

aplasia cutis [cleft palate - epidermolysis], ptosis [ectropion - thin skin - beaked nose], aplasia cutis congenital [cleft palate - epidermolysis bullosa - ectrodactyly], Aplasia cutis cleft palate epidermolysis, Ptosis, ectropion, thin skin, beaked nose, Aplasia cutis congenita, cleft palate, epidermolysis bullosa, and ectrodactyly

Aplasia cutis cleft palate epidermolysis, Aplasia cutis congenita, cleft palate, epidermolysis bullosa, and ectrodactyly, Ptosis, ectropion, thin skin, beaked nose
Source - Office of Rare Diseases (ORD) of the National Institutes of Health (NIH)

 

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