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...»

See full list of 34 symptoms of Orofaciodigital syndrome, type 3

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...»

Read more about treatments for Orofaciodigital syndrome, type 3

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.

More about prognosis of Orofaciodigital syndrome, type 3

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• What is Orofaciodigital syndrome, type 3?
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