X-LINKED SPINAL MUSCULAR-ATROPHY (KENNEDYS-SYNDROME) - A KINDRED WITH HYPOBETALIPOPROTEINEMIA

被引:25
作者
WARNER, CL
SERVIDEI, S
LANGE, DJ
MILLER, E
LOVELACE, RE
ROWLAND, LP
机构
[1] COLUMBIA PRESBYTERIAN MED CTR, INST NEUROL, DEPT NEUROL, NEW YORK, NY 10032 USA
[2] UNIV CATTOLICA SACRO CUORE, SCH MED, DEPT NEUROL, I-00168 ROME, ITALY
[3] LONG ISL JEWISH MED CTR, DEPT INTERNAL MED ENDOCRINOL, LEVITTOWN, NY USA
关键词
D O I
10.1001/archneur.1990.00530100087018
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Kennedy's syndrome, X-linked adultonset bulbospinal muscular atrophy, has been described in over 30 families. The characteristic distribution of weakness creates a recognizable syndrome, augmented by frequent findings of testicular atrophy and gynecomastia. Type IV or type II hyperlipoproteinemia has been found in some families. We have studied another family with Kennedy's syndrome, this one with hypobetalipoproteinemia. The diversity of serum patterns suggests that lipoprotein abnormalities are not causally related to either the endocrinopathy or the spinal muscular atrophy. However, gene linkage studies indicate proximity of the gene for Kennedy's syndrome and the gene encoding the androgen receptor, which could explain the combination of a motor neuron disorder and the endocrine abnormalities. © 1990, American Medical Association. All rights reserved.
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收藏
页码:1117 / 1120
页数:4
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