Sclerema Neonatorum [sclerema neonatorum]

topical
2
Persistent link   https://www.medvik.cz/link/D012593
Definition

A severe, sometimes fatal, disorder of adipose tissue occurring chiefly in preterm or debilitated infants suffering from an underlying illness and manifested by a diffuse, nonpitting induration of the affected tissue. The skin becomes cold, yellowish, mottled, and inflexible.

Annotation
a skin abnorm; adipose tissue dis in preterm or debilitated inf; do not use /congen & do not coord with INFANT, NEWBORN, DISEASES
DUI
D012593 MeSH Browser
CUI
M0019540

Allowable subheadings

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

C Diseases
C16 Congenital, Hereditary, and Neonatal Diseases and Abnormalities 439
C16.131 Congenital Abnormalities 1 753
C16.131.831 Skin Abnormalities 51
C16.131.831.066 Acrodermatitis 67
C16.131.831.108 Carney Complex 8
C16.131.831.150 Dyskeratosis Congenita 9
C16.131.831.350 Ectodermal Dysplasia 33
C16.131.831.428 Ehlers-Danlos Syndrome 51
C16.131.831.493 Epidermolysis Bullosa 108
C16.131.831.512 Ichthyosis 62
C16.131.831.580 Incontinentia Pigmenti 19
C16.131.831.675 Port-Wine Stain 5
C16.131.831.720 Prolidase Deficiency
C16.131.831.766 Pseudoxanthoma Elasticum 13
C16.131.831.775 Rothmund-Thomson Syndrome 8
C16.131.831.812 Sclerema Neonatorum 2
C16.131.831.874 Trichothiodystrophy Syndromes 1
C16.131.831.936 Xeroderma Pigmentosum 25
C16.614 Infant, Newborn, Diseases 1 950
C16.614.042 Amniotic Band Syndrome 6
C16.614.053 Anemia, Neonatal 22
C16.614.092 Asphyxia Neonatorum 173
C16.614.131 Birth Injuries 158
C16.614.166 Colic 125
C16.614.183 Congenital Bone Marrow Failure Syndromes 2
C16.614.200 Congenital Hyperinsulinism 24
C16.614.213 Cystic Fibrosis 1 330
C16.614.258 Epilepsy, Benign Neonatal 13
C16.614.304 Erythroblastosis, Fetal 140
C16.614.378 Hernia, Umbilical 45
C16.614.438 Hydrophthalmos 9
C16.614.451 Hyperbilirubinemia, Neonatal 65
C16.614.465 Hyperostosis, Cortical, Congenital 14
C16.614.492 Ichthyosis 62
C16.614.521 Infant, Premature, Diseases 318
C16.614.580 Meconium Aspiration Syndrome 35
C16.614.595 Mobius Syndrome 10
C16.614.610 Neonatal Abstinence Syndrome 75
C16.614.627 Neonatal Sepsis 35
C16.614.643 Nystagmus, Congenital 8
C16.614.660 OEIS Complex
C16.614.677 Ophthalmia Neonatorum 12
C16.614.694 Persistent Fetal Circulation Syndrome 17
C16.614.760 Rothmund-Thomson Syndrome 8
C16.614.810 Sclerema Neonatorum 2
C16.614.815 Severe Combined Immunodeficiency 64
C16.614.868 Syphilis, Congenital 87
C16.614.890 Thanatophoric Dysplasia 7
C16.614.899 Thrombocytopenia, Neonatal Alloimmune 14
C16.614.909 Toxoplasmosis, Congenital 75
C16.614.940 Vitamin K Deficiency Bleeding 22
C16.614.947 Wolman Disease 15
C17 Skin and Connective Tissue Diseases 32
C17.800 Skin Diseases 2 801
C17.800.804 Skin Abnormalities 51
C17.800.804.066 Acrodermatitis 67
C17.800.804.108 Anetoderma 5
C17.800.804.150 Dyskeratosis Congenita 9
C17.800.804.350 Ectodermal Dysplasia 33
C17.800.804.428 Ehlers-Danlos Syndrome 51
C17.800.804.493 Epidermolysis Bullosa 108
C17.800.804.512 Ichthyosis 62
C17.800.804.580 Incontinentia Pigmenti 19
C17.800.804.675 Port-Wine Stain 5
C17.800.804.766 Pseudoxanthoma Elasticum 13
C17.800.804.775 Rothmund-Thomson Syndrome 8
C17.800.804.812 Sclerema Neonatorum 2
C17.800.804.874 Trichothiodystrophy Syndromes 1
C17.800.804.936 Xeroderma Pigmentosum 25

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