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Diseases » Whelan syndrome » Summary

What is Whelan syndrome?

What is Whelan syndrome?

  • Whelan syndrome: A rare genetic disorder characterized by oral frenula, oral clefts, underdeveloped nose flaps, finger abnormalities and hydronephrosis.

Whelan syndrome: Introduction

Types of Whelan syndrome:

Broader types of Whelan syndrome:

What causes Whelan syndrome?

Causes of Whelan syndrome: see causes of Whelan syndrome

What are the symptoms of Whelan syndrome?

Symptoms of Whelan syndrome: see symptoms of Whelan syndrome

Whelan syndrome: Testing

Diagnostic testing: see tests for Whelan syndrome.

Misdiagnosis: see misdiagnosis and Whelan syndrome.

How is it treated?

Doctors and Medical Specialists for Whelan syndrome: Medical Geneticist ; see also doctors and medical specialists for Whelan syndrome.
Treatments for Whelan syndrome: see treatments for Whelan syndrome

Name and Aliases of Whelan syndrome

Main name of condition: Whelan syndrome

Other names or spellings for Whelan syndrome:

Oral facial digital syndrome Type VII, digito-orofacial syndrome VII, Orofaciodigital Syndrome VII, OFD7, OFDS VII

Whelan syndrome: Related Conditions

Research the causes of these diseases that are similar to, or related to, Whelan syndrome:


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