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What is Blethen-Wenick-Hawkins syndrome?

What is Blethen-Wenick-Hawkins syndrome?

  • Blethen-Wenick-Hawkins syndrome: A rare syndrome characterized mainly by short stature, skeletal abnormalities and reduced pituitary gland functioning.

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

Blethen-Wenick-Hawkins syndrome: Introduction

Types of Blethen-Wenick-Hawkins syndrome:

Broader types of Blethen-Wenick-Hawkins syndrome:

What causes Blethen-Wenick-Hawkins syndrome?

Causes of Blethen-Wenick-Hawkins syndrome: see causes of Blethen-Wenick-Hawkins syndrome

What are the symptoms of Blethen-Wenick-Hawkins syndrome?

Symptoms of Blethen-Wenick-Hawkins syndrome: see symptoms of Blethen-Wenick-Hawkins syndrome

Blethen-Wenick-Hawkins syndrome: Testing

Diagnostic testing: see tests for Blethen-Wenick-Hawkins syndrome.

Misdiagnosis: see misdiagnosis and Blethen-Wenick-Hawkins syndrome.

How is it treated?

Doctors and Medical Specialists for Blethen-Wenick-Hawkins syndrome: Pediatrician, Endocrinologist ; see also doctors and medical specialists for Blethen-Wenick-Hawkins syndrome.
Treatments for Blethen-Wenick-Hawkins syndrome: see treatments for Blethen-Wenick-Hawkins syndrome

Name and Aliases of Blethen-Wenick-Hawkins syndrome

Main name of condition: Blethen-Wenick-Hawkins syndrome

Other names or spellings for Blethen-Wenick-Hawkins syndrome:

hypopituitarism [dwarfism - skeletal anomalies], Hypopituitarism dwarfism skeletal anomalies

 

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