okulocerebrorenální syndrom [Oculocerebrorenal Syndrome]

tematický
9
Termíny

deficit fosfatidylinositol-4,5-bisfosfát-5-fosfatasy
deficit fosfatidylinozitol-4,5-bisfosfát-5-fosfatázy
Loweho nemoc
Loweho okulocerebrorenální syndrom
Loweho syndrom
Loweův syndrom
okulocerebrorenální dystrofie

 

Cerebro-Oculo-Renal Syndrome
Cerebrooculorenal Syndrome
Lowe Disease
Lowe Oculocerebrorenal Syndrome
Lowe Syndrome
Lowe-Bickel Syndrome
Lowe-Terrey-MacLachlan Syndrome
Oculocerebrorenal Dystrophy
Oculocerebrorenal Syndrome of Lowe
Phosphatidylinositol 4,5-Bisphosphate 5-Phosphatase Deficiency
Phosphatidylinositol-4,5-Bisphosphate-5-Phosphatase Deficiency
Renal-Oculocerebrodystrophy

Perzistentní odkaz   https://www.medvik.cz/link/D009800
Definice

X-vázané recesivní onemocnění charakterizované postižením očí, CNS a ledvin. Mezi klinické příznaky patří vrozená katarakta, mentální retardace a renální tubulární dysfunkce (Fanconiho syndrom, renální tubulární acidóza, hypofosfatemie vázaná na chromozom X čili vitamin D-rezistentní rachitis) a dále skolióza. Tento stav je vyvolaný deficitem fosfatidylinositol-4,5-bisfosfát-5-fosfatasy, který vede k poruchám metabolismu fosfatidylinositolu a signální dráhy inositolu.

A sex-linked recessive disorder affecting multiple systems including the EYE, the NERVOUS SYSTEM, and the KIDNEY. Clinical features include congenital CATARACT; MENTAL RETARDATION; and renal tubular dysfunction (FANCONI SYNDROME; RENAL TUBULAR ACIDOSIS; X-LINKED HYPOPHOSPHATEMIA or vitamin-D-resistant rickets) and SCOLIOSIS. This condition is due to a deficiency of phosphatidylinositol 4,5-bisphosphate-5-phosphatase leading to defects in PHOSPHATIDYLINOSITOL metabolism and INOSITOL signaling pathway. (from Menkes, Textbook of Child Neurology, 5th ed, p60; Am J Hum Genet 1997 Jun;60(6):1384-8)

DUI
D009800 MeSH Prohlížeč
CUI
M0015215
Předchozí užití
Abnormalities, Multiple (1968-1976); Eye Diseases (1966-1976); Kidney Diseases (1966-1976)
Historická pozn.
1991(1977)
Veřejná pozn.
1991; see RENAL TUBULAR TRANSPORT, INBORN ERRORS 1977-1990

C Nemoci
C10.228.140 nemoci mozku 1 177
C10.228.140.163 metabolické nemoci mozku 84
C10.228.140.163.100.084 adrenoleukodystrofie 41
C10.228.140.163.100.320 galaktosemie 44
C10.228.140.163.100.355 Hartnupova nemoc 2
C10.228.140.163.100.360 hepatolentikulární degenerace 243
C10.228.140.163.100.362 dědičné demyelinizační nemoci CNS 11
C10.228.140.163.100.365 homocystinurie 107
C10.228.140.163.100.375 neketotická hyperglycinemie 7
C10.228.140.163.100.380 hyperlysinemie
C10.228.140.163.100.412 Leighova nemoc 26
C10.228.140.163.100.425 Leschův-Nyhanův syndrom 20
C10.228.140.163.100.520 nemoc s močí javorového sirupu 8
C10.228.140.163.100.535 syndrom MELAS 17
C10.228.140.163.100.540 Menkesova choroba 12
C10.228.140.163.100.545 syndrom MERRF 4
C10.228.140.163.100.593 nedostatek mevalonátkinázy 16
C10.228.140.163.100.640 okulocerebrorenální syndrom 9
C10.228.140.163.100.687 fenylketonurie 285
C10.228.140.163.100.725 nedostatek pyruvátkarboxylázy
C10.228.140.163.100.813 Refsumova nemoc 6
C10.228.140.163.100.844 Refsumova nemoc infantilní
C10.228.140.163.100.875 tyrosinemie 18
C10.228.140.163.100.937 vrozené poruchy cyklu močoviny 7
C10.228.140.163.100.968 Zellwegerův syndrom 10
C12.050.351.968 urologické nemoci 834
C12.050.351.968.419 nemoci ledvin 3 059
C12.050.351.968.419.815.093 renální tubulární acidóza 59
C12.050.351.968.419.815.279 Bartterův syndrom 19
C12.050.351.968.419.815.364 Dentova choroba 1
C12.050.351.968.419.815.450 Fanconiho syndrom 23
C12.050.351.968.419.815.491 Gitelmanův syndrom 17
C12.050.351.968.419.815.532 renální glykosurie 36
C12.050.351.968.419.815.647 familiární hypofosfatemie 12
C12.050.351.968.419.815.683 Liddleův syndrom 4
C12.050.351.968.419.815.720 okulocerebrorenální syndrom 9
C12.050.351.968.419.815.770 pseudohypoaldosteronismus 9
C12.050.351.968.419.815.885 renální aminoacidurie 27
C12.200.777 urologické nemoci 834
C12.200.777.419 nemoci ledvin 3 059
C12.200.777.419.815.093 renální tubulární acidóza 59
C12.200.777.419.815.279 Bartterův syndrom 19
C12.200.777.419.815.364 Dentova choroba 1
C12.200.777.419.815.450 Fanconiho syndrom 23
C12.200.777.419.815.491 Gitelmanův syndrom 17
C12.200.777.419.815.532 renální glykosurie 36
C12.200.777.419.815.647 familiární hypofosfatemie 12
C12.200.777.419.815.683 Liddleův syndrom 4
C12.200.777.419.815.720 okulocerebrorenální syndrom 9
C12.200.777.419.815.770 pseudohypoaldosteronismus 9
C12.200.777.419.815.885 renální aminoacidurie 27
C12.950.419 nemoci ledvin 3 059
C12.950.419.815.093 renální tubulární acidóza 59
C12.950.419.815.279 Bartterův syndrom 19
C12.950.419.815.364 Dentova choroba 1
C12.950.419.815.450 Fanconiho syndrom 23
C12.950.419.815.491 Gitelmanův syndrom 17
C12.950.419.815.532 renální glykosurie 36
C12.950.419.815.647 familiární hypofosfatemie 12
C12.950.419.815.683 Liddleův syndrom 4
C12.950.419.815.720 okulocerebrorenální syndrom 9
C12.950.419.815.770 pseudohypoaldosteronismus 9
C12.950.419.815.885 renální aminoacidurie 27
C16.131 vrozené vady 1 740
C16.131.077.019 syndrom delece 22q11 2
C16.131.077.065 Alagillův syndrom 19
C16.131.077.095 Angelmanův syndrom 35
C16.131.077.121 Barthův syndrom 6
C16.131.077.137 Bloomův syndrom 11
C16.131.077.229 Carneyův komplex 8
C16.131.077.245 ciliopatie 9
C16.131.077.250 Cockayneův syndrom 4
C16.131.077.256 Costellův syndrom 3
C16.131.077.272 de Langeové syndrom 4
C16.131.077.299 hluchoslepota 65
C16.131.077.313 Donohueův syndrom 1
C16.131.077.327 Downův syndrom 510
C16.131.077.350 ektodermální dysplazie 33
C16.131.077.371 Fraserův syndrom 2
C16.131.077.393 Gardnerův syndrom 20
C16.131.077.401 heterotaxe 7
C16.131.077.410 holoprosencefalie 8
C16.131.077.445 incontinentia pigmenti 19
C16.131.077.537 Loeysův-Dietzův syndrom 7
C16.131.077.550 Marfanův syndrom 105
C16.131.077.578 Moebiův syndrom 10
C16.131.077.592 moniletrichosis 1
C16.131.077.619 Nethertonův syndrom 2
C16.131.077.696 Cantrellova pentalogie 1
C16.131.077.703 POEMS syndrom 34
C16.131.077.730 Praderův-Williho syndrom 91
C16.131.077.735 nedostatek prolidázy
C16.131.077.740 Proteův syndrom 8
C16.131.077.745 prune belly syndrom 3
C16.131.077.790 zarděnky vrozené 20
C16.131.077.889 Sotosův syndrom 4
C16.131.077.919 Patauův syndrom 6
C16.131.077.929 syndrom trizomie 18 5
C16.131.077.938 Waardenburgův syndrom 10
C16.131.077.970 Zellwegerův syndrom 10
C16.320.051 Alagillův syndrom 19
C16.320.100 Brugadův syndrom 40
C16.320.129 CADASIL 8
C16.320.165 CHARGE syndrom 1
C16.320.170 cherubismus 1
C16.320.184 ciliopatie 9
C16.320.188 Costellův syndrom 3
C16.320.190 cystická fibróza 1 328
C16.320.215 Donohueův syndrom 1
C16.320.240 nanismus 97
C16.320.306 syndrom Frasier
C16.320.314 deficit GATA2 1
C16.320.322.030 Aicardiho syndrom
C16.320.322.068 Barthův syndrom 6
C16.320.322.092 choroideremie 3
C16.320.322.100 Dentova choroba 1
C16.320.322.108 dyskeratosis congenita 9
C16.320.322.124 Fabryho nemoc 187
C16.320.322.201 glykogenóza typu IIb 11
C16.320.322.217 glykogenóza typu VIII
C16.320.322.235 hemofilie B 214
C16.320.365 hemoglobinopatie 68
C16.320.467 Kallmannův syndrom 10
C16.320.488 laminopatie 2
C16.320.540 Marfanův syndrom 105
C16.320.565.151.355 Hartnupova nemoc 2
C16.320.565.151.600 okulocerebrorenální syndrom 9
C16.320.565.189.084 adrenoleukodystrofie 41
C16.320.565.189.320 galaktosemie 44
C16.320.565.189.355 Hartnupova nemoc 2
C16.320.565.189.360 hepatolentikulární degenerace 243
C16.320.565.189.365 homocystinurie 107
C16.320.565.189.375 neketotická hyperglycinemie 7
C16.320.565.189.380 hyperlysinemie
C16.320.565.189.412 Leighova nemoc 26
C16.320.565.189.425 Leschův-Nyhanův syndrom 20
C16.320.565.189.535 syndrom MELAS 17
C16.320.565.189.540 Menkesova choroba 12
C16.320.565.189.545 syndrom MERRF 4
C16.320.565.189.593 nedostatek mevalonátkinázy 16
C16.320.565.189.640 okulocerebrorenální syndrom 9
C16.320.565.189.687 fenylketonurie 285
C16.320.565.189.813 Refsumova nemoc 6
C16.320.565.189.844 Refsumova nemoc infantilní
C16.320.565.189.875 tyrosinemie 18
C16.320.565.189.968 Zellwegerův syndrom 10
C16.320.577 svalové dystrofie 140
C16.320.728 osteochondrodysplazie 123
C16.320.812 pyknodysostóza 2
C16.320.831.271 Dentova choroba 1
C16.320.831.450 Fanconiho syndrom 23
C16.320.831.491 Gitelmanův syndrom 17
C16.320.831.532 renální glykosurie 36
C16.320.831.698 Liddleův syndrom 4
C16.320.831.770 pseudohypoaldosteronismus 9
C16.320.831.885 renální aminoacidurie 27
C16.320.925 Wernerův syndrom 14
C18.452 metabolické nemoci 1 196
C18.452.132.100.084 adrenoleukodystrofie 41
C18.452.132.100.320 galaktosemie 44
C18.452.132.100.355 Hartnupova nemoc 2
C18.452.132.100.360 hepatolentikulární degenerace 243
C18.452.132.100.365 homocystinurie 107
C18.452.132.100.375 neketotická hyperglycinemie 7
C18.452.132.100.380 hyperlysinemie
C18.452.132.100.412 Leighova nemoc 26
C18.452.132.100.425 Leschův-Nyhanův syndrom 20
C18.452.132.100.535 syndrom MELAS 17
C18.452.132.100.540 Menkesova choroba 12
C18.452.132.100.545 syndrom MERRF 4
C18.452.132.100.593 nedostatek mevalonátkinázy 16
C18.452.132.100.640 okulocerebrorenální syndrom 9
C18.452.132.100.687 fenylketonurie 285
C18.452.132.100.813 Refsumova nemoc 6
C18.452.132.100.844 Refsumova nemoc infantilní
C18.452.132.100.875 tyrosinemie 18
C18.452.132.100.968 Zellwegerův syndrom 10
C18.452.648.151.355 Hartnupova nemoc 2
C18.452.648.151.600 okulocerebrorenální syndrom 9
C18.452.648.189.084 adrenoleukodystrofie 41
C18.452.648.189.320 galaktosemie 44
C18.452.648.189.355 Hartnupova nemoc 2
C18.452.648.189.360 hepatolentikulární degenerace 243
C18.452.648.189.365 homocystinurie 107
C18.452.648.189.375 neketotická hyperglycinemie 7
C18.452.648.189.380 hyperlysinemie
C18.452.648.189.412 Leighova nemoc 26
C18.452.648.189.425 Leschův-Nyhanův syndrom 20
C18.452.648.189.535 syndrom MELAS 17
C18.452.648.189.540 Menkesova choroba 12
C18.452.648.189.545 syndrom MERRF 4
C18.452.648.189.593 nedostatek mevalonátkinázy 16
C18.452.648.189.640 okulocerebrorenální syndrom 9
C18.452.648.189.687 fenylketonurie 285
C18.452.648.189.813 Refsumova nemoc 6
C18.452.648.189.844 Refsumova nemoc infantilní
C18.452.648.189.875 tyrosinemie 18
C18.452.648.189.968 Zellwegerův syndrom 10