Lamellar ichthyosis. The natural clinical course of collodion baby

1968 ◽  
Vol 97 (1) ◽  
pp. 3-13 ◽  
Author(s):  
C. L. Lentz
Keyword(s):  
Clinical Course ◽  
Lamellar Ichthyosis ◽  
Collodion Baby

Collodion baby (lamellar ichthyosis)

1969 ◽  
Vol 100 (2) ◽  
pp. 249-250
Author(s):  
B. Schwimmer
Keyword(s):  
Lamellar Ichthyosis ◽  
Collodion Baby

scholarly journals A Case Report on Congenital Ichthyosis - Collodion Baby

2016 ◽  
Vol 11 (1) ◽  
pp. 39-42
Author(s):  
Md Kamrul Hassan ◽  
Aloke Kumar Saha ◽  
Poly Begum ◽  
Tahmina Akter ◽  
Shyamol Kumar Saha
Keyword(s):  
Case Report ◽  
Initial Phase ◽  
Severe Form ◽  
Clinical Entity ◽  
Self Healing ◽  
Lamellar Ichthyosis ◽  
Congenital Ichthyosis ◽  
Ichthyosis Vulgaris ◽  
Collodion Baby ◽  
Lamellar Type

Collodion baby describes a highly characteristic clinical entity in newborns encased in a yellowish translucent membrane resembling collodion. In most cases the condition either precedes the development of one of a variety of ichthyoses, the commonest of which are lamellar ichthyosis and non-bullous ichthyosiform erythroderma, or occasionally represents an initial phase of other ichthyoses such as ichthyosis vulgaris. In at least 10% of all cases of collodion baby, the condition is followed by a mild ichthyosis of lamellar type, so mild as to be considered more or less normal, so-called self-healing collodion baby or 'lamellar ichthyosis of the newborn'. In this report, we present a severe form of ichthyosis.Faridpur Med. Coll. J. Jan 2016;11(1): 39-42

scholarly journals Congenital Lamellar Icthyosis (Collodion Baby)

2011 ◽  
Vol 31 (3) ◽  
pp. 257
Author(s):  
B Baghel
Keyword(s):  
Skin Disorder ◽  
Lamellar Ichthyosis ◽  
Congenital Ichthyosis ◽  
Collodion Baby

Lamellar ichthyosis, also known as ichthyosis lammellaris and nonbullous congenital ichthyosis, is a rare inherited skin disorder, affecting around 1 in 600,000 people the images of this rare variety of skin disorder has been presented here. DOI: http://dx.doi.org/10.3126/jnps.v31i3.3769 J Nep Paedtr Soc 2011;31(3): 257

Lamellar Ichthyosis

1981 ◽  
Vol 2 (7) ◽  
pp. 213-216
Author(s):  
Nils Olof Sandberg
Keyword(s):  
Autosomal Recessive ◽  
Skin Diseases ◽  
Recessive Trait ◽  
Autosomal Recessive Trait ◽  
Clinical Genetic ◽  
Lamellar Ichthyosis ◽  
Congenital Ichthyosis ◽  
Healthy Pregnancy ◽  
Collodion Baby

Congenital ichthyoses represent a heterogeneous group of rare skin diseases. The disorders are heritable and have in common a varying degree of hyperkeratosis. During the years there has been much confusion regarding the classification of the ichthyoses. Today we have a classification based on clinical, genetic, cellular, and kinetic observations (Table). 1,2 Most patients fit into one of the four major types of ichthyoses. Beside those major types, congenital ichthyosis may be seen as part of several uncommon syndromes. The most often seen congenital ichthyosis is the lamellartype which is inherited as an autosomal recessive trait.3 Lamellar ichthyosis was first described by Seeligmann under the title of "epidermal desquamation of the newborn" in 1841.4 Lentz and Altman reviewed the literature in 1968 and found a total of 103 cases.5 CASE HISTORY A.S., a 2,720-gm infant was born at 37 weeks of gestation. His parents and a brother are healthy. Pregnancy and labor were uncomplicated. Apgar scores at one and five minutes were 10. At birth the infant was encased in a shiny collodion membrane. Because of the tight envelope his nose, ears, fingers, and toes were whitish, and the baby could hardly move. The lips and eyelids were everted. The diagnosis of collodion baby was made immediately (Figs 1 and 2).

scholarly journals Collodion Baby - a Case Report

2014 ◽  
Vol 6 (4) ◽  
pp. 186-190
Author(s):  
Vesna Stojanović ◽  
Aleksandra Doronjski ◽  
Slobodan Spasojević ◽  
Nataša Stašuk ◽  
Anica Radulović
Keyword(s):  
Case Report ◽  
Initial Phase ◽  
Rare Case ◽  
Clinical Entity ◽  
Self Healing ◽  
Normal Appearance ◽  
Lamellar Ichthyosis ◽  
Ichthyosis Vulgaris ◽  
Collodion Baby ◽  
Lamellar Type

Abstract Colloidon baby describes a highly characteristic clinical entity in newborns encased in a yellowish translucent membrane resembling collodion. In most cases the condition either precedes the development of one of a variety of ichthyoses, the commonest of which are lamellar ichthyosis and non-bullous ichthyosiform erythroderma, or occasionally represents an initial phase of other ichthyoses such as ichthyosis vulgaris. In at least 10% of all cases of collodion baby, the condition is followed by a mild ichthyosis of lamellar type, so mild as to be considered more or less normal, so-called self-healing collodion baby or ‘lamellar ichthyosis of the newborn’. In this report we present a rare case of collodion baby in whom, after collodion membrane peeled-off, the skin retained normal appearance.

scholarly journals 'Collodion baby': Presentation of a rare form of familial lamellar ichthyosis

2016 ◽  
Vol 50 (3) ◽  
pp. 110-114
Author(s):  
Marina Stanojevic ◽  
Tanja Stojkovic ◽  
Dragana Savic ◽  
Biljana Vuletic ◽  
Andjelka Stojkovic ◽  
...  
Keyword(s):  
Rare Form ◽  
Lamellar Ichthyosis ◽  
Collodion Baby

Lamellar ichthyosis in a collodion baby caused by CYP4F22 mutations in a non-consanguineous family outside the Mediterranean

2013 ◽  
Vol 72 (2) ◽  
pp. 193-195 ◽  
Author(s):  
Kazumitsu Sugiura ◽  
Takuya Takeichi ◽  
Kana Tanahashi ◽  
Yasutomo Ito ◽  
Tomoki Kosho ◽  
...  
Keyword(s):  
Consanguineous Family ◽  
Lamellar Ichthyosis ◽  
Collodion Baby ◽  
The Mediterranean

Collodion baby and lamellar ichthyosis

1998 ◽  
Vol 25 (2) ◽  
pp. 116-121 ◽  
Author(s):  
Brian Sandler ◽  
Ken Hashimoto
Keyword(s):  
Lamellar Ichthyosis ◽  
Collodion Baby
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