PRASENILE DEMENZ BEI XERODERMA PIGMENTOSUM

D. Dorndorf; K. Wessel; P. Vieregge; R. Verleger; D. Kompf

PRASENILE DEMENZ BEI XERODERMA PIGMENTOSUM

D. Dorndorf, K. Wessel, P. Vieregge, R. Verleger, D. Kompf

Klinik für Neurologie

Abstract

Neurological manifestations of xeroderma pigmentosum, a rare autosomal recessive neurocutaneous syndrome, are variable. The association with progressive mental retardation, usually with onset in childhood, is well known. We present a case of x.p. with progressive presenile dementia. This combination has, to our knowledge, not yet been reported in the literature. Although no hints on another aetiology have been found, the coincidental combination of x.p. with M. Alzheimer has to be taken into consideration. CT scan and MRI showed a marked cerebral atrophy.

Titel in Übersetzung	Presenile dementia in a case of Xeroderma pigmentosum
Originalsprache	Deutsch
Zeitschrift	Nervenarzt
Jahrgang	62
Ausgabenummer	10
Seiten (von - bis)	641-644
Seitenumfang	4
ISSN	0028-2804
Publikationsstatus	Veröffentlicht - 01.01.1991

UN SDGs

Dieser Output leistet einen Beitrag zu folgendem(n) Ziel(en) für nachhaltige Entwicklung

SDG 3 – Gesundheit und Wohlergehen
SDG 10 – Weniger Ungleichheiten

Strategische Forschungsbereiche und Zentren

Forschungsschwerpunkt: Gehirn, Hormone, Verhalten - Center for Brain, Behavior and Metabolism (CBBM)

Weitere Links

Link to publication in Scopus

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abstract = "Neurological manifestations of xeroderma pigmentosum, a rare autosomal recessive neurocutaneous syndrome, are variable. The association with progressive mental retardation, usually with onset in childhood, is well known. We present a case of x.p. with progressive presenile dementia. This combination has, to our knowledge, not yet been reported in the literature. Although no hints on another aetiology have been found, the coincidental combination of x.p. with M. Alzheimer has to be taken into consideration. CT scan and MRI showed a marked cerebral atrophy.",

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T1 - PRASENILE DEMENZ BEI XERODERMA PIGMENTOSUM

AU - Dorndorf, D.

AU - Wessel, K.

AU - Vieregge, P.

AU - Verleger, R.

AU - Kompf, D.

PY - 1991/1/1

Y1 - 1991/1/1

N2 - Neurological manifestations of xeroderma pigmentosum, a rare autosomal recessive neurocutaneous syndrome, are variable. The association with progressive mental retardation, usually with onset in childhood, is well known. We present a case of x.p. with progressive presenile dementia. This combination has, to our knowledge, not yet been reported in the literature. Although no hints on another aetiology have been found, the coincidental combination of x.p. with M. Alzheimer has to be taken into consideration. CT scan and MRI showed a marked cerebral atrophy.

AB - Neurological manifestations of xeroderma pigmentosum, a rare autosomal recessive neurocutaneous syndrome, are variable. The association with progressive mental retardation, usually with onset in childhood, is well known. We present a case of x.p. with progressive presenile dementia. This combination has, to our knowledge, not yet been reported in the literature. Although no hints on another aetiology have been found, the coincidental combination of x.p. with M. Alzheimer has to be taken into consideration. CT scan and MRI showed a marked cerebral atrophy.

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AN - SCOPUS:0025996812

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