Disease #05112 (HMN2 (neuropathy, motor, distal, hereditary, type II (HMN-2)))

Official abbreviation HMN2
Name neuropathy, motor, distal, hereditary, type II (HMN-2)
OMIM ID -
Inheritance -
Individuals reported having this disease 5
Phenotype entries for this disease 5
Associated with 0 genes -
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Disease features -
Remarks -
Date created 2016-01-11 01:38:35 +01:00 (CET)
Date last edited 2021-12-11 13:56:28 +01:00 (CET)


Individuals

5 entries on 1 page. Showing entries 1 - 5.
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00056460 - PubMed: Ikeda 2009 3-generation family, 3 affected males M no Japan - - - - - HMN2 see paper; ... HSPB1 HSPB1 1 3 Johan den Dunnen
00056466 - PubMed: Irobi 2004 4-generation family, 8 affecteds (3F, 5M) F;M no United Kingdom (Great Britain) - - - - - HMN2 Neuropathy, distal hereditary motor, type II HSPB8 HSPB8 1 8 Johan den Dunnen
00056467 - PubMed: Irobi 2004 6-generation family, 34 affecteds (16F, 18M) F;M no Czech Republic - - - - - HMN2 neuropathy, distal hereditary motor, type II HSPB8 HSPB8 1 34 Johan den Dunnen
00057160 - PubMed: Irobi 2004 4-generation family, 4 affecteds (2F, 2M) F;M no Bulgaria - - - - - HMN2 Neuropathy, distal hereditary motor, type II HSPB8 HSPB8 1 4 Johan den Dunnen
00057161 - PubMed: Irobi 2004 6-generation family, 32 affecteds (13F, 19M) F;M no Belgium - - - - - HMN2 neuropathy, distal hereditary motor, type II; exclusive lower motor neuron disease without sensory loss, onset age 15–25y, presenting symptoms paresis extensor muscles big toe later extensor muscles feet, disease progresses rapidly, complete paralysis all distal muscles lower extremities within 5y, EMG chronic neurogenic alterations HSPB8 HSPB8 1 32 Johan den Dunnen
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