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The Neuropsychiatry of Adrenomyeloneuropathy
CNS Spectrums, 2007ABSTRACTBackground: While the adult form of adrenoleukodystrophy (ALD) has been associated with an elevated rate of affective disturbance, the myeloneuropathic form of the disease known as adrenomyeloneuropathy (AMN) has been associated with only occasional cases of major mental illness.
Mark A, Walterfang +3 more
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Journal of Neurology, 1982
Adrenomyeloneuropathy (AMN) is reported in two kindreds. In the first family, four male patients were affected: two adults with the full clinical picture but with a different chronology of the main symptoms, a third adult with central nervous system involvement and a child who died early with adrenal insufficiency.
J J, Martin +3 more
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Adrenomyeloneuropathy (AMN) is reported in two kindreds. In the first family, four male patients were affected: two adults with the full clinical picture but with a different chronology of the main symptoms, a third adult with central nervous system involvement and a child who died early with adrenal insufficiency.
J J, Martin +3 more
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Adrenomyeloneuropathy—report on a family
Journal of Internal Medicine, 1991Abstract. A family is reported in which there is one case of adrenomyeloneuropathy, one case of Addison's disease and at least three heterozygous females with spastic paraparesis and peripheral neuropathy. Adrenomyeloneuropathy has not been reported previously in Scandinavia.
B H, Holmberg, E, Hägg, L, Hagenfeldt
exaly +3 more sources
Testicular dysfunction in adrenomyeloneuropathy
European Journal of Endocrinology, 1997Adrenomyeloneuropathy (AMN) is a disorder due to a disturbance in the peroxisomal beta-oxidation of saturated very long chain fatty acids. It is characterized by symptoms of the nervous as well as the endocrine systems, especially the adrenal cortex and the gonads. We investigated the testicular function in 49 male AMN patients aged 36.2 +/- 1.5 years (
W, Brennemann +3 more
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Acta Neuropathologica, 1980
Histopathological, immunocytochemical, and electron microscopical investigations were carried out in a man with a protracted history of spastic paraparesis, adrenal insufficiency and hypogonadism. Pathological findings were identical with those of the few previously reported cases of adrenomyeloneuropathy (AMN) including cytoplasmic lamellar inclusions
A, Probst +3 more
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Histopathological, immunocytochemical, and electron microscopical investigations were carried out in a man with a protracted history of spastic paraparesis, adrenal insufficiency and hypogonadism. Pathological findings were identical with those of the few previously reported cases of adrenomyeloneuropathy (AMN) including cytoplasmic lamellar inclusions
A, Probst +3 more
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Comptes rendus des seances de la Societe de biologie et de ses filiales, 1981
An adrenomyeloneuropathy is observed in a patient died at 24 years old after an illness of five years duration. These case is peculiar by the presence of lamellar cytoplasmic inclusions in the Schwann cells. Adrenomyeloneuropathy is an adult variant of adrenoleucodystrophy.
J, Julien +4 more
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An adrenomyeloneuropathy is observed in a patient died at 24 years old after an illness of five years duration. These case is peculiar by the presence of lamellar cytoplasmic inclusions in the Schwann cells. Adrenomyeloneuropathy is an adult variant of adrenoleucodystrophy.
J, Julien +4 more
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Somatosensory evoked potentials in adrenomyeloneuropathy
Neurology, 1997Adrenomyeloneuropathy (AMN) is an X-linked metabolic disorder causing accumulation of very-long-chain fatty acids with multifocal nervous system demyelination of the peripheral nerves, spinal cord, and cerebrum. The extent to which the disorder affects upper versus lower limbs or peripheral versus CNS has not been electrophysiologically defined in a ...
P W, Kaplan +3 more
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The Journal of the Association of Physicians of India, 2005
Adrenomyeloneuropathy is a rare X-linked inherited disorder of peroxisomes characterized by the accumulation of very long chain fatty acids (VLCFA) in the central and peripheral nervous system, adrenal glands and testis leading to the dysfunction of these organs and systems.
M M, Mehndiratta +3 more
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Adrenomyeloneuropathy is a rare X-linked inherited disorder of peroxisomes characterized by the accumulation of very long chain fatty acids (VLCFA) in the central and peripheral nervous system, adrenal glands and testis leading to the dysfunction of these organs and systems.
M M, Mehndiratta +3 more
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Occurrence of adrenocortical insufficiency in adrenomyeloneuropathy
Neurology, 1996Adrenoleukodystrophy and its clinical variant adrenomyeloneuropathy (AMN) are disorders due to peroxisomal degradation of very-long-chain fatty acids (VLCFA). Both forms are characterized by CNS involvement and variable involvement of endocrine functions, especially the adrenal cortex.
W, Brennemann +3 more
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Micturitional disturbance in a patient with adrenomyeloneuropathy (AMN)
Neurourology and Urodynamics, 1998We report a case of adrenomyeloneuropathy (AMN) in which serial urodynamic studies showed neurogenic bladder dysfunction. The patient was in good health until the age of 12, when he began to lose his hair. At age 25 he started to have urinary urgency, difficulty in voiding, occasional fecal incontinence, erectile impotence, and progressive gait ...
Ryuji Sakakibara +2 more
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