01060nas a2200265 4500000000100000008004100001260001300042653001000055653002200065653001800087653005000105653001100155653000900166653001300175653001500188100001500203700001500218700001600233700001300249245008800262300001000350490000700360520041300367022001400780 1984 d c1984 Dec10aAdult10aDiseases in Twins10aFoot Diseases10aHereditary Sensory and Autonomic Neuropathies10aHumans10aMale10aPedigree10aSkin Ulcer1 aBerginer V1 aBaruchin A1 aBen-Yakar Y1 aMahler D00aPlantar ulcers in hereditary sensory neuropathy. A plea for conservative treatment. a664-80 v233 a
Hereditary sensory neuropathy is a rare syndrome characterized by the occurrence, in childhood or early adult life, of perforating ulcers of the feet, lightning pains, and loss of cutaneous sensation and tendon reflexes in the lower extremities. Three patients with hereditary sensory neuropathy were family members. Trophic ulcers may be caused by diseases other than diabetes, syphilis, and leprosy.
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