Results 61 to 70 of about 737 (185)

Genodermatoses

open access: yesJournal of Pharmacy and Bioallied Sciences, 2015
Genodermatoses are an inherited disorder, present with multisystem involvement. Help us to identify regular mutations and appalling skin diseases with recessive inheritance.
N Aravindha Babu   +3 more
doaj   +1 more source

Diffuse palmoplantar keratoderma, onychodystrophy, universal hypotrichosis and cysts [PDF]

open access: yes, 2017
No abstract ...
Mohammad Adil   +3 more
core   +1 more source

Dental Management of Ectodermal Dysplasia Syndrome at an Early Age: A Case Report [PDF]

open access: yes, 2019
Objectives: Ectodermal dysplasia (ED) is a relatively common sex-linked dermatitis characterized by congenital dysplasia of one or more ectodermal structures and their accessory appendages.
Ansari, Ghasem   +2 more
core   +2 more sources

Hidrotic Ectodermal Dysplasia with Ichthyosiform Erythroderma-like Skin Changes -An Autopsy Case- [PDF]

open access: yes, 1984
We present an autopsy case of 30-day-old female infant who had hidrotic ectodermal dyplasia with ichthyosiform erythroderma-like skin changes and low value of migration test of neutrophils.
Kawai Kioko   +5 more
core   +1 more source

EDA Missense Variant in a Cat with X-Linked Hypohidrotic Ectodermal Dysplasia. [PDF]

open access: yes
Hypohidrotic ectodermal dysplasia is a developmental defect characterized by sparse or absent hair, missing or malformed teeth and defects in eccrine glands. Loss-of-function variants in the X-chromosomal EDA gene have been reported to cause hypohidrotic
Chevallier, Lucie   +5 more
core   +2 more sources

Ectodermal dysplasia and partial anodontia: A case report [PDF]

open access: yes, 2015
Ectodermal dysplasia is a hereditary disorder that occurs as a consequence of disturbances in the ectoderm of the developing embryo. It is usually accompanied by lack of sweat glands and a partial or complete absence of primary and/or permanent dentition.
Prasad M
core   +1 more source

Congenital atrichia with papular lesions [PDF]

open access: yes, 2020
Congenital atrichia with papular lesions is a rare, autosomal recessive and irreversible form of total alopecia of the body hair characterized by hair loss soon after birth and the development of keratinfilled cysts or horny papules over extensive areas ...
Gavali, Sujit   +3 more
core  

The role of gap junctions in inflammatory and neoplastic disorders (Review). [PDF]

open access: yes, 2017
Gap junctions are intercellular channels made of connexin proteins, mediating both electrical and biochemical signals between cells. The ability of gap junction proteins to regulate immune responses, cell proliferation, migration, apoptosis and ...
Chan, Yin Wah Fiona   +4 more
core   +2 more sources

Zygomatic Implant Survival in 9 Ectodermal Dysplasia Patients with 3.5 to 7-year Follow Up [PDF]

open access: yes, 2020
Ectodermal dysplasia syndrome is a complex group of genetic disorders identified by the abnormal development of the ectodermal structures. The aim of this retrospective clinical case series report was to evaluate the outcomes of the ectodermal dysplasia ...
E. Grecchi   +4 more
core   +1 more source

Oral rehabilitation with removable dental prosthesis in a six-year-old patient with hypohidrotic ectodermal dysplasia [PDF]

open access: yes, 2017
Introduction: Ectodermal dysplasia is an abnormality of the ectoderm and its derivatives, phenotypically expressed in males and genetically inherited from mothers.
Brancher, João Armando   +5 more
core   +2 more sources

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