1 linically confused with hereditary neuralgic amyotrophy.

2 short stature, cognitive deficits and distal amyotrophy.

3 ome new information in the areas of diabetic amyotrophy and diabetic autonomic neuropathy will also b

4 omal dominant disorders hereditary neuralgic amyotrophy and tylosis with esophageal cancer.

5 aracterized by slow progression, distal limb amyotrophy, and pyramidal tract signs associated with se

6 med this disinhibition-dementia-parkinsonism-amyotrophy complex.

7 cally by disinhibition-dementia-parkinsonism-amyotrophy complex.

8  recently localized the hereditary neuralgic amyotrophy gene to the distal long arm of chromosome 17

9                         Hereditary neuralgic amyotrophy (HNA) is an autosomal dominant disorder assoc

10   Germline mutations in hereditary neuralgic amyotrophy (HNA) map to the region which is common to th

11 (MTs) and is mutated in hereditary neuralgic amyotrophy (HNA), an autosomal-dominant neuropathy.

12  The molecular basis of hereditary neuralgic amyotrophy is unknown and the specific gene which leads

13 pathy (DLSRPN) (other names include diabetic amyotrophy) is well recognized, unlike the non-diabetic

14 issense mutation (JNPL3) develop progressive amyotrophy, neurofibrillary degeneration, and neuronal l

15 ect for IgM anti-MAG neuropathy and diabetic amyotrophy (radiculoplexus neuropathy) is lacking.

16                         Hereditary neuralgic amyotrophy with predilection for the brachial plexus is

17  signs including distal motor neuropathy and amyotrophy with severe selective ulnar nerve involvement