Results 11 to 20 of about 2,089 (158)

Lower Lid Ectropion in Hypohidrotic Ectodermal Dysplasia [PDF]

Case Reports in Ophthalmological Medicine, 2015
We report a case of a lower lid ectropion with ectodermal dysplasia and ectropion blepharoplasty surgery experience. A 14-year-old Han nationality male patient with typical characteristics of hypohidrotic ectodermal dysplasia presented to our clinic for ...
Xiaoyun Zhang, Li Xu, Xiaofang Li, Chunyan Li, Haitao Zhang   +4 more
doaj   +2 more sources

Dental management of hypohidrotic ectodermal dysplasia: A report of two cases

Contemporary Clinical Dentistry, 2015
Ectodermal dysplasia (ED) represents a group of inherited conditions characterized by anomalies in two or more structures of ectodermal origin, which can be presented as problems related to hair, nail, teeth, sweat glands, and sebaceous glands.
Meenu Mittal, Dhirendra Srivastava, Ashok Kumar, Poonam Sharma   +3 more
doaj   +2 more sources

A case report of hypohidrotic ectodermal dysplasia: A mini-review with latest updates

Journal of Family Medicine and Primary Care, 2018
Ectodermal dysplasia (ED) is a rare hereditary disorder involving two or more of the ectodermal structures, which include the skin, hair, nails, teeth, and sweat glands. The two most common forms of the disease are hypohidrotic/anhidrotic ED and hidrotic
Girish Gulab Meshram, Neeraj Kaur, Kanwaljeet Singh Hura   +2 more
doaj   +2 more sources

HED (Hypohidrotic Ectodermal Dysplasia): A Review [PDF]

, 2021
The ectodermal dysplasias (EDs) are a heterogeneous group of inherited, developmental disorders characterized by alterations in two or more ectodermal structures including the hair, teeth, nails and sweat glands.
Callea M., Willoughby C.E., Bashyam M.D., Scalisi F.C., Yavuz I., Dogan M.S.   +5 more
core   +9 more sources

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

Genes (Basel)
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
Rietmann SJ, Cochet-Faivre N, Dropsy H, Jagannathan V, Chevallier L, Leeb T.   +5 more
europepmc   +3 more sources

Hypohidrotic ectodermal dysplasia

, 2023
Ectodermal dysplasia (ED); is a rare disorder affecting ectodermal derivatives i.e. skin, nails, teeth, hair and sweat glands. It is divided into many subtypes. Among those, two major types involve (a) Hypohidrotic /Anhidrotic ED (Christ-Siemens-Touraine
Zahida Rani, Faryal Naveed, Zareen Saqib Suleri, Alina Amjad   +3 more
core   +1 more source

Hypohidrotic Ectodermal Dysplasia: a rare inherited multisystem disorder [PDF]

, 2021
Hypohidrotic ectodermal dysplasia (HED), also known as Christ-Siemens-Touraine syndrome, is a rare X-linked genetic disorder characterized by the faulty development of the ectodermal structures, resulting in most notably anhydrosis/ hypohidrosis ...
Srinithi, R ; Sree Balaji Medical College and Hospital, Bharath Institute of Higher Education and Research, Chennai, Tamil Nadu, India, Ramya, R, Sundari, S   +2 more
core   +1 more source

Customized Prosthetic Oral Rehabilitation of a Child with Hypohidrotic Ectodermal Dysplasia: A Case Report [PDF]

Journal of South Asian Association of Pediatric Dentistry
The present case report describes interdisciplinary prosthetic oral rehabilitation of a 7-year-old male child presenting classical features of hypohidrotic ectodermal dysplasia (HED) and subtotal anodontia. The treatment, in this case, was simplified and
Hitesh Chander Mittal, Sudhir Bhandari, Ashima Goyal, Aditi Kapur, Krishan Gauba   +4 more
doaj   +1 more source

Exome sequencing enables diagnosis of X-linked hypohidrotic ectodermal dysplasia in patient with eosinophilic esophagitis and severe atopy

Allergy, Asthma & Clinical Immunology, 2021
X-linked hypohidrotic ectodermal dysplasia (XLHED) is the most common form of ectodermal dysplasia. Clinical and genetic heterogeneity between different ectodermal dysplasia types and evidence of incomplete penetrance and variable expressivity increase ...
Bhavi P. Modi, Kate L. Del Bel, Susan Lin, Mehul Sharma, Phillip A. Richmond, Clara D. M. van Karnebeek, Edmond S. Chan, Vishal Avinashi, Wingfield E. Rehmus, Catherine M. Biggs, Wyeth W. Wasserman, Stuart E. Turvey   +11 more
doaj   +1 more source

Ectodermal dysplasia

Česká Stomatologie a Praktické Zubní Lékařství, 2013
Background: Ectodermal dysplasia is a rare, genetically determined disease, which is characterized by alterations in two or more ectodermal structures, at least one of these involving alterations in hair, teeth, nails, or sweat glands.
L. Kramerová, E. Kaplová
doaj   +1 more source