Pelizaeus-Merzbacher Disease [Pelizaeusova-Merzbacherova nemoc]

topical
11
Terms

Cockaynova-Pelizaeusova-Merzbacherova nemoc
Pelizaeusova-Merzbacherova nemoc klasická forma
Pelizaeusova-Merzbacherova nemoc, atypická forma
Pelizaeusova-Merzbacherova nemoc, dospělá forma
Pelizaeusova-Merzbacherova nemoc, přechodná forma

 

Adult Pelizaeus-Merzbacher Disease
Atypical Pelizaeus-Merzbacher Disease
Classic Pelizaeus-Merzbacher Disease
Cockayne-Pelizaeus-Merzbacher Disease
Leukodystrophy, Hypomyelinating, 1
Pelizaeus-Merzbacher Brain Sclerosis
Pelizaeus-Merzbacher Disease, Adult
Pelizaeus-Merzbacher Disease, Atypical
Pelizaeus-Merzbacher Disease, Classic
Pelizaeus-Merzbacher Disease, Transitional
Pelizaeus-Merzbacher Sclerosis, Brain
Transitional Pelizaeus-Merzbacher Disease

Persistent link   https://www.medvik.cz/link/D020371
Definition

A rare, slowly progressive disorder of myelin formation. Subtypes are referred to as classic, congenital, transitional, and adult forms of this disease. The classic form is X-chromosome linked, has its onset in infancy and is associated with a mutation of the proteolipid protein gene. Clinical manifestations include TREMOR, spasmus nutans, roving eye movements, ATAXIA, spasticity, and NYSTAGMUS, CONGENITAL. Death occurs by the third decade of life. The congenital form has similar characteristics but presents early in infancy and features rapid disease progression. Transitional and adult subtypes have a later onset and less severe symptomatology. Pathologic features include patchy areas of demyelination with preservation of perivascular islands (trigoid appearance). (From Menkes, Textbook of Child Neurology, 5th ed, p190)

DUI
D020371 MeSH Browser
CUI
M0003895
Previous indexing
Diffuse Cerebral Sclerosis of Schilder (1966-1999); Multiple Sclerosis (1966-1999)
History note
2000; use CEREBRAL SCLEROSIS, DIFFUSE 1979-1999
Public note
2000; see CEREBRAL SCLEROSIS, DIFFUSE 1979-1999

C Diseases
C10.228.140 Brain Diseases 1 177
C10.228.140.163 Brain Diseases, Metabolic 84
C10.228.140.163.100.362.250 Adrenoleukodystrophy 41
C10.228.140.163.100.362.312 Alexander Disease 6
C10.228.140.163.100.362.375 Canavan Disease 9
C10.228.140.163.100.362.500 Leukodystrophy, Globoid Cell 16
C10.228.140.163.100.362.550 Leukodystrophy, Metachromatic 29
C10.228.140.163.100.362.775 Pelizaeus-Merzbacher Disease 11
C10.228.140.695 Leukoencephalopathies 11
C10.228.140.695.625.250 Adrenoleukodystrophy 41
C10.228.140.695.625.312 Alexander Disease 6
C10.228.140.695.625.375 Canavan Disease 9
C10.228.140.695.625.500 Leukodystrophy, Globoid Cell 16
C10.228.140.695.625.550 Leukodystrophy, Metachromatic 29
C10.228.140.695.625.775 Pelizaeus-Merzbacher Disease 11
C10.314.400.250 Adrenoleukodystrophy 41
C10.314.400.312 Alexander Disease 6
C10.314.400.375 Canavan Disease 9
C16.320.322.030 Aicardi Syndrome
C16.320.322.068 Barth Syndrome 6
C16.320.322.092 Choroideremia 3
C16.320.322.100 Dent Disease 1
C16.320.322.108 Dyskeratosis Congenita 9
C16.320.322.124 Fabry Disease 187
C16.320.322.186 Focal Dermal Hypoplasia 6
C16.320.322.235 Hemophilia B 214
C16.320.322.241 Ichthyosis, X-Linked 9
C16.320.322.562 Muscular Dystrophy, Duchenne 133
C16.320.322.937 Wiskott-Aldrich Syndrome 20
C16.320.565.189.362.250 Adrenoleukodystrophy 41
C16.320.565.189.362.312 Alexander Disease 6
C16.320.565.189.362.375 Canavan Disease 9
C16.320.565.189.362.500 Leukodystrophy, Globoid Cell 16
C16.320.565.189.362.550 Leukodystrophy, Metachromatic 29
C16.320.565.189.362.775 Pelizaeus-Merzbacher Disease 11
C18.452 Metabolic Diseases 1 196
C18.452.132.100.362.250 Adrenoleukodystrophy 41
C18.452.132.100.362.312 Alexander Disease 6
C18.452.132.100.362.375 Canavan Disease 9
C18.452.132.100.362.500 Leukodystrophy, Globoid Cell 16
C18.452.132.100.362.550 Leukodystrophy, Metachromatic 29
C18.452.132.100.362.775 Pelizaeus-Merzbacher Disease 11
C18.452.648.189.362.250 Adrenoleukodystrophy 41
C18.452.648.189.362.312 Alexander Disease 6
C18.452.648.189.362.375 Canavan Disease 9
C18.452.648.189.362.500 Leukodystrophy, Globoid Cell 16
C18.452.648.189.362.550 Leukodystrophy, Metachromatic 29
C18.452.648.189.362.775 Pelizaeus-Merzbacher Disease 11