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Orofaciodigital syndrome, type 3

Orofaciodigital syndrome, type 3: Introduction

Orofaciodigital syndrome, type 3: A rare genetic disorder characterized by oral frenula, oral clefts, underdeveloped nose flaps and finger, teeth and eye abnormalities. More detailed information about the symptoms, causes, and treatments of Orofaciodigital syndrome, type 3 is available below.

Symptoms of Orofaciodigital syndrome, type 3

  • Extra little fingers
  • Extra little toes
  • Excess mouth frenuli
  • Enlarged mouth frenuli
  • Multiple mouth frenuli
  • more symptoms...»

Treatments for Orofaciodigital syndrome, type 3

  • Treatment varies depending on the type and severity of symptom that develop:
  • Surgery may be needed to correct defects or abnormalities e.g. cleft lip
  • Access to programs and services as required e.g. physical therapy, speech therapy, educational support, social, vocational and medical services
  • Various symptomatic and supportive measures as required
  • Genetic counseling and joining a support group is recommended
  • more treatments...»

Home Diagnostic Testing

Home medical testing related to Orofaciodigital syndrome, type 3:

Wrongly Diagnosed with Orofaciodigital syndrome, type 3?

Orofaciodigital syndrome, type 3: Complications

Read more about complications of Orofaciodigital syndrome, type 3.

Causes of Orofaciodigital syndrome, type 3

Read more about causes of Orofaciodigital syndrome, type 3.

Orofaciodigital syndrome, type 3: Undiagnosed Conditions

Commonly undiagnosed diseases in related medical categories:

Misdiagnosis and Orofaciodigital syndrome, type 3

Leg cramps at night a classic sign: The symptom of having leg muscle cramps, particularly at night, is a classic sign of undiagnosed diabetes. However, there are also various other causes. See causes...read more »

Orofaciodigital syndrome, type 3: Research Doctors & Specialists

Research related physicians and medical specialists:

Other doctor, physician and specialist research services:

Orofaciodigital syndrome, type 3: Animations

Prognosis for Orofaciodigital syndrome, type 3

Prognosis for Orofaciodigital syndrome, type 3: The prognosis varies depending on the type and severity of symptoms that develop. Prompt diagnosis and appropriate treatment can improve prognosis and quality of life.

Statistics for Orofaciodigital syndrome, type 3

Orofaciodigital syndrome, type 3: Broader Related Topics

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Definitions of Orofaciodigital syndrome, type 3:

A syndrome of eye abnormalities, lobulated hamartomatous tongue, dental abnormalities, bifid uvula, postaxial hexadactyly, pectus excavatum, short sternum, kyphosis, mental retardation, and ceaseless ("see-saw") winking of the eyelids occurring in one of the two sisters in the original report. - (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, type 3 as a "rare disease".
Source - Orphanet

Related Orofaciodigital syndrome, type 3 Info

More information about Orofaciodigital syndrome, type 3

  1. Orofaciodigital syndrome, type 3: Introduction
  2. Symptoms
  3. Causes
  4. Treatments
  5. Misdiagnosis
  6. Home Testing
  7. Complications
  8. Prognosis
 

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