Ichthyosis, Lamellar [lamelární ichtyóza]

topical
22
Terms

collodion baby
erythrodermia ichthyosiformis nonbullosa
erythrodermia ichthyosiformis nonbullosa congenitalis
harlekýn fetus
harlequin ichthyosis
harlequin ichtyóza
ichthyosis congenita
ichthyosis congenita typu I
ichthyosis congenita typu II
ichtyosis lamellosa
ichtyóza lamelární
kolodiové dítě
lamelární ichtyózy
nebulózní kongenitální ichtyoziformní erytrodermie
plod harlekýn
vrozená ichtyóza

 

Collodion Baby Syndrome
Collodion Fetus
Congenital Ichthyosiform Erythroderma, Nonbullous
Congenital Nonbullous Ichthyosiform Erythroderma
Desquamation of Newborn
Erythroderma Ichthyosiforme, Nonbullous
Harlequin Baby Syndrome
Harlequin Fetus
Harlequin Ichthyosis
Ichthyoses, Lamellar
Ichthyosiform Erythroderma, Nonbullous Congenital
Ichthyosis Congenita
Ichthyosis Congenita I
Ichthyosis Congenita II
Ichthyosis, Lamellar, 1
Lamellar Exfoliation of Newborn
Lamellar Ichthyoses
Lamellar Ichthyosis
Lamellar Ichthyosis, Type 1
Nonbullous Congenital Ichthyosiform Erythroderma
Nonbullous Congenital Lamellar Ichthyosis

Persistent link   https://www.medvik.cz/link/D017490
Definition

A chronic, congenital ichthyosis inherited as an autosomal recessive trait. Infants are usually born encased in a collodion membrane which sheds within a few weeks. Scaling is generalized and marked with grayish-brown quadrilateral scales, adherent at their centers and free at the edges. In some cases, scales are so thick that they resemble armored plate.

Annotation
do not coord with INFANT, NEWBORN, DISEASES
nekombinuj s deskriptorem NEMOCI NOVOROZENCŮ
DUI
D017490 MeSH Browser
CUI
M0026532
Previous indexing
Ichthyosiform Erythroderma, Congenital (1991-1992); Ichthyosis (1966-1992)
History note
1993; use ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL 1991-1992; ERYTHRODERMA ICHTHYOSIFORME, NONBULLOUS use ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL 1991-1992, use ICHTHYOSIS 1979-1990
Public note
1993; see ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL 1991-1992; ERYTHRODERMA ICHTHYOSIFORME, NONBULLOUS see ICHTHYOSIFORM ERYTHRODERMA, CONGENITAL 1991-1992, see ICHTHYOSIS 1979-1990

C Diseases
C16.131.831 Skin Abnormalities 51
C16.131.831.512 Ichthyosis 62
C16.131.831.512.400.375 Hyperkeratosis, Epidermolytic 20
C16.131.831.512.400.410 Ichthyosis, Lamellar 22
C16.131.831.512.400.705 Netherton Syndrome 2
C16.320.850.400.375 Hyperkeratosis, Epidermolytic 20
C16.320.850.400.410 Ichthyosis, Lamellar 22
C16.614.492 Ichthyosis 62
C16.614.492.400.375 Hyperkeratosis, Epidermolytic 20
C16.614.492.400.410 Ichthyosis, Lamellar 22
C16.614.492.400.705 Netherton Syndrome 2
C17.800 Skin Diseases 2 801
C17.800.428 Keratosis 133
C17.800.428.333 Ichthyosis 62
C17.800.428.333.250.375 Hyperkeratosis, Epidermolytic 20
C17.800.428.333.250.410 Ichthyosis, Lamellar 22
C17.800.428.333.250.705 Netherton Syndrome 2
C17.800.804 Skin Abnormalities 51
C17.800.804.512 Ichthyosis 62
C17.800.804.512.400.375 Hyperkeratosis, Epidermolytic 20
C17.800.804.512.400.410 Ichthyosis, Lamellar 22
C17.800.804.512.400.705 Netherton Syndrome 2
C17.800.827.400.375 Hyperkeratosis, Epidermolytic 20
C17.800.827.400.410 Ichthyosis, Lamellar 22

Harlequin type ichthyosis Disease MeSH Browser

Ichthyosiform erythroderma, Brocq congenital, nonbullous form Disease MeSH Browser

Ichthyosiform erythroderma, corneal involvement, deafness Disease MeSH Browser

Ichthyosis, Lamellar, 5 Disease MeSH Browser

Lamellar ichthyosis, autosomal dominant form Disease MeSH Browser

Lamellar ichthyosis, type 2 Disease MeSH Browser

Lamellar ichthyosis, type 3 Disease MeSH Browser

Self-Healing Collodion Baby Disease MeSH Browser