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What is Neurofibromatosis type 3A?

What is Neurofibromatosis type 3A?

  • Neurofibromatosis type 3A: A rare genetic disorder characterized by areas of increased and decreased skin pigmentation and the development of many non-cancerous nerve and skin tumors some of which may eventually become malignant. The skin tumors tend to develop characteristically on the palms of the hands.

Neurofibromatosis type 3A: Introduction

Types of Neurofibromatosis type 3A:

Broader types of Neurofibromatosis type 3A:

How serious is Neurofibromatosis type 3A?

Prognosis of Neurofibromatosis type 3A: the condition can result in rapid death if multiple tumors develop in the central nervous system

What causes Neurofibromatosis type 3A?

Causes of Neurofibromatosis type 3A: see causes of Neurofibromatosis type 3A

What are the symptoms of Neurofibromatosis type 3A?

Symptoms of Neurofibromatosis type 3A: see symptoms of Neurofibromatosis type 3A

Neurofibromatosis type 3A: Testing

Diagnostic testing: see tests for Neurofibromatosis type 3A.

Misdiagnosis: see misdiagnosis and Neurofibromatosis type 3A.

How is it treated?

Doctors and Medical Specialists for Neurofibromatosis type 3A: Medical Geneticist, Neurologist ; see also doctors and medical specialists for Neurofibromatosis type 3A.
Treatments for Neurofibromatosis type 3A: see treatments for Neurofibromatosis type 3A

Name and Aliases of Neurofibromatosis type 3A

Main name of condition: Neurofibromatosis type 3A

Other names or spellings for Neurofibromatosis type 3A:

Neurofibromatosis type 3, NF3A, neurofibromatosis, type II, mixed central and peripheral, neurofibromatosis, type III of Riccardi, NF IIIA, Neurofibromatosis, Type 3, mixed central and peripheral, Neurofibromatosis, Type 3, Riccardi type, NF 3

 

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