Orofaciodigital syndrome type1

Orofaciodigital syndrome type1:

Orofaciodigital syndrome type1: Introduction

Orofaciodigital syndrome type1: A rare genetic disorder characterized by variable malformations of the face, digits and inside the mouth. Type 1 is distinguished from the other types of this condition by the presence of polycystic kidneys and a X-linked dominant inheritance. More detailed information about the symptoms, causes, and treatments of Orofaciodigital syndrome type1 is available below.

Symptoms of Orofaciodigital syndrome type1

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See full list of 27 symptoms of Orofaciodigital syndrome type1

Home Diagnostic Testing

Home medical testing related to Orofaciodigital syndrome type1:

Vision & Eye Health: Home Testing:
- Home Eye Tests
- Home Vision Tests
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Wrongly Diagnosed with Orofaciodigital syndrome type1?

Misdiagnosis of Orofaciodigital syndrome type1

Orofaciodigital syndrome type1: Complications

Causes of Orofaciodigital syndrome type1

Less Common Symptoms of Orofaciodigital syndrome type1

See full list of 16 occasional symptoms of Orofaciodigital syndrome type1

Orofaciodigital syndrome type1: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Vision & Eye: serious diseases often undiagnosed:
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Misdiagnosis and Orofaciodigital syndrome type1

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Orofaciodigital syndrome type1: Research Doctors & Specialists

Research related physicians and medical specialists:

Ear, Nose & Throat Specialists:
Eye Health Specialists (Ophthalmology):
- Ophthalmology (Eye Specialist)
Arthritis & Joint Health Specialists (Rheumatology):
- Rheumatology (Joint Health)
- Pediatric Rheumatology (Child Joint Health)
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Other doctor, physician and specialist research services:

Orofaciodigital syndrome type1: Animations

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Statistics for Orofaciodigital syndrome type1

Orofaciodigital syndrome type1: Broader Related Topics

Types of Orofaciodigital syndrome type1

User Interactive Forums

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Definitions of Orofaciodigital syndrome type1:

Abnormalities of the orodental, facial, renal, and digital structures occurring in various combinations and frequently associated with retarded mental development. Patients in the original report were all females, except for the case with Klinefelter syndrome - (Source - Diseases Database)

Ophanet, a consortium of European partners, currently defines a condition rare when it affects 1 person per 2,000. They list Orofaciodigital syndrome type1 as a "rare disease".
Source - Orphanet

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