Neurofibromatosis

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Template:DiseaseDisorder infobox (Template:ICDO) |

 ICD9        = Template:ICD9 |

}} Neurofibromatosis is a autosomal dominant genetic disorder.

1 Types
2 Symptoms
3 Genetics and Hereditability
4 Family
5 History
6 External links
7 Notes
8 References

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Types

There are two major forms:

Neurofibromatosis type I (was known as Von Recklinghausen disease after Friedrich Daniel von Recklinghausen). Incidence is 1:3000.

Neurofibromatosis type II (or "MISME Syndrome"). Incidence is 1:40,000.

Schwannomatosis is a rare form that is clinically and genetically distinct from types I and II. Multiple schwannomas (rather than neurofibromas) occur, and about one-third of patients have these tumors in only one part of the body. The vestibular nerve is spared. Pain is the primary symptom, although numbness, tingling and weakness can also occur.

Six other, extremely rare, forms are also recognized:
- OMIM 162210
- OMIM 162220
- OMIM 162240
- OMIM 162260
- OMIM 162270
- OMIM 601321

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Symptoms

Neurofibromatosis type 1 - mutation on chromosome 17

multiple neurofibromas on the skin and under the skin
various other skin phenomena such as freckling of the groin and the arm pit
a predisposition to particular tumors (both benign and malignant)
the presence of 6 or more Café au lait spots (pigmented birthmarks) may suggest the presence of this condition
skeletal abnormalities such as scoliosis or bowing of the legs might occur
lisch nodules (iris nevi)- a hamartoma of iris
tumor on the optic nerve

Image:Neurofibromatosis plexiform neurofriboma 3.jpg

Neurofibromatosis type 2 - mutation on chromosome 22

bilateral tumors, acoustic neuromas on the vestibulocochlear nerve
the hallmark of NF 2 is hearing loss due to acoustic neuromas around the age of twenty
the tumors may cause:
- headache
- balance problems
- facial weakness/paralysis
- patients with NF2 may also develop other brain tumors, as well as spinal tumors

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Genetics and Hereditability

Neurofibromatosis type 1 is due to mutation on chromosome 17q , the gene product being Neurofibromin ( a GTPase activating enzyme).<ref>Fauci,et al Harrison's Principle of Internal Medicine 16th Ed. p 2453 </ref>

Neurofibromatosis type 2 is due to mutation on chromosome 22q , the gene product is Merlin, a cytoskeletal protein.

Both NF1 and NF2 are autosomal dominant disorders, meaning that only one copy of the mutated gene need be inherited to pass the disorder. A child of a parent with NF1 or NF2 and an unaffected parent will have a 50% chance of inheriting the disorder.

Complicating the question of heritability is the distiction between genotype and phenotype, that is, between the genetics and the actual manifestation of the disorder. In the case of NF1, no clear links between genotype and phenotype have been found, and the severity and specific nature of the symptoms may vary widely among family members with the disorder (Korf and Rubenstein 2005). In the case of NF2, however, manifestations are similar among family members; a strong genotype-phenotype correlation is believed to exist (ibid).

Both NF1 and NF2 can also appear spontaneously through random mutation, with no family history. These spontaneous or sporadic cases account for about one half of neurofibromatosis cases (ibid).

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Family

Neurofibromatosis is considered a member of the neurocutaneous syndromes (phakomatoses). In addition to the types of neurofibromatosis, the phakomatoses also include tuberous sclerosis, Sturge-Weber syndrome and von Hippel-Lindau disease. This grouping is an artifact of an earlier time in medicine, before the distinct genetic basis of each of these diseases was understood.

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History

Image:Elephantman1.jpg Joseph Merrick, the Elephant Man, was once considered to have been afflicted with either elephantiasis or neurofibromatosis type I. However, it is now generally believed that Merrick suffered from the very rare Proteus syndrome.

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