Cutis Laxa [cutis laxa]

topical
10
Terms

dermatolysis
dermatolýza
dermatomegalie
dermolysis
dermolýza
volná kůže

 

Dermatolysis
Dermatomegaly

Persistent link   https://www.medvik.cz/link/D003483
Definition

A group of connective tissue diseases in which skin hangs in loose pendulous folds. It is believed to be associated with decreased elastic tissue formation as well as an abnormality in elastin formation. Cutis laxa is usually a genetic disease, but acquired cases have been reported. (From Dorland, 27th ed)

Annotation
do not confuse with ANETODERMA; CUTIS LAXA is mostly a genetic disease: both are described as "loose skin"
DUI
D003483 MeSH Browser
CUI
M0005430
History note
1968; use DERMATOLYSIS 1963-1967
Public note
1968; sww DERMATOLYSIS 1963-1967

Allowable subheadings

BL
blood
CF
cerebrospinal fluid
CI
chemically induced
CL
classification
CO
complications 2
CN
congenital
DI
diagnosis 6
DG
diagnostic imaging
DH
diet therapy
DT
drug therapy
EC
economics
EM
embryology
EN
enzymology
EP
epidemiology
EH
ethnology
ET
etiology 1
GE
genetics 4
HI
history
IM
immunology
ME
metabolism 1
MI
microbiology
MO
mortality
NU
nursing
PS
parasitology
PA
pathology 1
PP
physiopathology
PC
prevention & control
PX
psychology
RT
radiotherapy
RH
rehabilitation
SU
surgery
TH
therapy 1
UR
urine
VE
veterinary
VI
virology

C Diseases
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.320 Genetic Diseases, Inborn 1 213
C16.320.850 Skin Diseases, Genetic 89
C16.320.850.080 Albinism 17
C16.320.850.180 Cutis Laxa 10
C16.320.850.190 Darier Disease 26
C16.320.850.210 Dermatitis, Atopic 1 445
C16.320.850.235 Dyskeratosis Congenita 9
C16.320.850.250 Ectodermal Dysplasia 33
C16.320.850.260 Ehlers-Danlos Syndrome 51
C16.320.850.275 Epidermolysis Bullosa 108
C16.320.850.337 Erythrokeratodermia Variabilis 1
C16.320.850.368 Hyaline Fibromatosis Syndrome 1
C16.320.850.400 Ichthyosiform Erythroderma, Congenital 8
C16.320.850.402 Ichthyosis Bullosa of Siemens 3
C16.320.850.405 Ichthyosis Vulgaris 5
C16.320.850.408 Ichthyosis, X-Linked 9
C16.320.850.420 Incontinentia Pigmenti 19
C16.320.850.475 Keratoderma, Palmoplantar 15
C16.320.850.542 Leukokeratosis, Hereditary Mucosal 1
C16.320.850.595 Lipoid Proteinosis of Urbach and Wiethe 5
C16.320.850.647 Monilethrix 1
C16.320.850.673 Netherton Syndrome 2
C16.320.850.700 Pemphigus, Benign Familial 11
C16.320.850.730 Porokeratosis 11
C16.320.850.738 Porphyria, Erythropoietic 11
C16.320.850.742 Porphyrias, Hepatic 26
C16.320.850.746 Prolidase Deficiency
C16.320.850.750 Pseudoxanthoma Elasticum 13
C16.320.850.765 Rothmund-Thomson Syndrome 7
C16.320.850.820 Sjogren-Larsson Syndrome 4
C16.320.850.895 Trichothiodystrophy Syndromes 1
C16.320.850.970 Xeroderma Pigmentosum 25
C17 Skin and Connective Tissue Diseases 32
C17.300 Connective Tissue Diseases 281
C17.300.116 Anetoderma 5
C17.300.182 Cartilage Diseases 140
C17.300.185 Cellulitis 132
C17.300.200 Collagen Diseases 183
C17.300.230 Cutis Laxa 10
C17.300.250 Dermatomyositis 239
C17.300.270 Dupuytren Contracture 61
C17.300.349 Fibromatosis, Plantar
C17.300.428 Homocystinuria 107
C17.300.451 Lipedema 20
C17.300.475 Lupus Erythematosus, Cutaneous 76
C17.300.480 Lupus Erythematosus, Systemic 1 091
C17.300.500 Marfan Syndrome 105
C17.300.540 Mixed Connective Tissue Disease 22
C17.300.550 Mucinoses 17
C17.300.680 Neoplasms, Connective Tissue 122
C17.300.690 Noonan Syndrome 52
C17.300.705 Osteopoikilosis 6
C17.300.710 Panniculitis 42
C17.300.715 Penile Induration 48
C17.300.766 Pseudoxanthoma Elasticum 13
C17.300.775 Rheumatic Diseases 2 175
C17.300.787 Scleroderma, Localized 61
C17.300.799 Scleroderma, Systemic 483
C17.300.849 Undifferentiated Connective Tissue Diseases 3
C17.300.899 Weill-Marchesani Syndrome 1
C17.800 Skin Diseases 2 799
C17.800.827 Skin Diseases, Genetic 89
C17.800.827.080 Albinism 17
C17.800.827.180 Cutis Laxa 10
C17.800.827.190 Darier Disease 26
C17.800.827.210 Dermatitis, Atopic 1 445
C17.800.827.235 Dyskeratosis Congenita 9
C17.800.827.250 Ectodermal Dysplasia 33
C17.800.827.260 Ehlers-Danlos Syndrome 51
C17.800.827.275 Epidermolysis Bullosa 108
C17.800.827.337 Erythrokeratodermia Variabilis 1
C17.800.827.368 Hereditary Autoinflammatory Diseases 46
C17.800.827.384 Hyaline Fibromatosis Syndrome 1
C17.800.827.400 Ichthyosiform Erythroderma, Congenital 8
C17.800.827.403 Ichthyosis Bullosa of Siemens 3
C17.800.827.405 Ichthyosis Vulgaris 5
C17.800.827.408 Ichthyosis, X-Linked 9
C17.800.827.420 Incontinentia Pigmenti 19
C17.800.827.475 Keratoderma, Palmoplantar 15
C17.800.827.595 Leukokeratosis, Hereditary Mucosal 1
C17.800.827.602 Monilethrix 1
C17.800.827.610 Muir-Torre Syndrome 10
C17.800.827.655 Netherton Syndrome 2
C17.800.827.700 Pemphigus, Benign Familial 11
C17.800.827.730 Porokeratosis 11
C17.800.827.738 Porphyria, Erythropoietic 11
C17.800.827.742 Porphyrias, Hepatic 26
C17.800.827.750 Pseudoxanthoma Elasticum 13
C17.800.827.775 Rothmund-Thomson Syndrome 7
C17.800.827.820 Sjogren-Larsson Syndrome 4
C17.800.827.895 Trichothiodystrophy Syndromes 1
C17.800.827.970 Xeroderma Pigmentosum 25

Cutis Laxa With Severe Pulmonary, Gastrointestinal, And Urinary Abnormalities Disease MeSH Browser

Cutis Laxa, Autosomal Dominant Disease MeSH Browser

Cutis Laxa, Autosomal Recessive, Type I Disease MeSH Browser

Cutis Laxa, Autosomal Recessive, Type IIA Disease MeSH Browser

Cutis Laxa, Autosomal Recessive, Type IIB Disease MeSH Browser

Cutis Laxa-Marfanoid Syndrome Disease MeSH Browser

De Barsy syndrome Disease MeSH Browser

Generalized elastolysis Disease MeSH Browser

Hemolytic Anemia, Congenital, with Emphysema and Cutis Laxa Disease MeSH Browser

Macrocephaly, Alopecia, Cutis Laxa, and Scoliosis Disease MeSH Browser

Occipital horn syndrome Disease MeSH Browser

SCARF syndrome Disease MeSH Browser

Wrinkly skin syndrome Disease MeSH Browser

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