Results 61 to 70 of about 8,965 (166)

Dupilumab Reduces Pruritus in Twins With Sjögren–Larsson Syndrome

open access: yesPediatric Dermatology, Volume 43, Issue 2, Page 395-397, March/April 2026.
ABSTRACT Sjögren–Larsson Syndrome (SLS), now termed ALDH3A2‐syndromic epidermal differentiation disorder (sEDD), is a rare genetic disorder marked by thickened skin, spasticity, and intellectual disability. Intractable pruritus is a nearly universal and debilitating feature of SLS that remains poorly managed by current therapies. We describe 4‐year‐old
Kennedy Gallagher   +3 more
wiley   +1 more source

Unraveling the intersection of sleep disorders and erectile dysfunction: Outcomes from two EPISONO editions

open access: yesAndrology, Volume 14, Issue 2, Page 385-397, February 2026.
Abstract Background There is growing interest in the relationship between sleep disorders and erectile dysfunction. We present the results from a 2015 follow‐up study in relation to the 2007 edition of Epidemiologic Sleep Study (EPISONO), a population‐based sleep study conducted in São Paulo, Brazil, and from the 4th edition of EPISONO (2018), with ...
Monica Levy Andersen   +4 more
wiley   +1 more source

Successful Treatment of an Adult with Atopic Dermatitis and Lamellar Ichthyosis Using Dupilumab

open access: yesBiologics: Targets & Therapy, 2022
Faisal K Binkhonain, Sara Aldokhayel, Hessah BinJadeed, Abdulaziz Madani Dermatology Department, College of Medicine, King Saud University, Riyadh, Saudi ArabiaCorrespondence: Abdulaziz Madani, Dermatology Department, King Saud University, Riyadh, 7805 ...
Binkhonain FK   +3 more
doaj  

Bébé pas comme les autres

open access: yesThe Pan African Medical Journal, 2014
Le bébé collodion est un aspect clinique grave caractérisé par une peau luisante, tendue et vernissée; une membrane rigide responsable d'un syndrome dysmorphique.
Nada El Moussaoui, Fatima Jabouirik
doaj   +1 more source

Exome Analysis Identifies a Novel Compound Heterozygous Alteration in TGM1 Gene Leading to Lamellar Ichthyosis in a Child From Saudi Arabia: Case Presentation

open access: yesFrontiers in Pediatrics, 2019
Background: Lamellar ichthyosis is an autosomal recessive type of rare skin disorders characterized with defective epidermis leading hyperkeratosis with brownish-gray scales over the body.
Sami Raja Alallasi   +11 more
doaj   +1 more source

Hypernatremia in two collodion babies

open access: yesThe Turkish Journal of Pediatrics, 1989
Two cases of collodion babies with hypernatremia are presented, and the importance of this electrolyte abnormality in skin disorders is also stressed.
U Soyuer   +3 more
doaj  

A Clinical Course And Follow Up Of Two Collodion Babies

open access: yesIndian Journal of Dermatology, 2001
Two collodion babies were followed clinically. One of the babies expired due to inadequate management while the other child survived due to combined efforts of paediatricians and dermatologists.
Jain Chanchal   +4 more
doaj  

A retrospective study on 16 collodion babies

open access: yesThe Turkish Journal of Pediatrics, 1997
Sixteen collodion babies followed in the Neonatal Care Unit between January 1982 and December 1994 were evaluated retrospectively. The preterm/term ratio was 1.6, and complete shedding of the collodion membrane took an average of 21.9 days (range ...
A Oztürk   +3 more
doaj  

Collodion Baby with TGM1 gene mutation

open access: yesInternational Medical Case Reports Journal, 2015
Deepak Sharma,1 Basudev Gupta,2 Sweta Shastri,3 Aakash Pandita,1 Smita Pawar4 1Department of Neonatology, Fernandez Hospital, Hyderguda, Hyderabad, Andhra Pradesh, 2Department of Pediatrics, Civil Hospital, Palwal, Haryana, 3Department of Pathology, NKP ...
Sharma D   +4 more
doaj  

Collodion Skin of the Newborn [PDF]

open access: yesArchives of Disease in Childhood, 1954
O D, FISHER, K G, McKEE
openaire   +2 more sources

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