Results 1 to 10 of about 128,250 (259)

Nail involvement in patients with epidermolysis bullosa: A systematic review [PDF]

Skin Health and Disease, 2023
Background Nail changes in patients with congenital epidermolysis bullosa (EB) are caused by abnormalities of the nail matrix and bed secondary to pathogenic alterations of the dermoepidermal junction.
Elena Pastrana‐Arellano, Diana Morales‐Olvera, María T. García‐Romero   +2 more
doaj   +3 more sources

Nail Abnormalities in Scabies Patients: A Systematic Review [PDF]

Clinical, Cosmetic and Investigational Dermatology
Hendra Gunawan, Risa Miliawati Nurul Hidayah, Pati Aji Achdiat, Retno Hesty Maharani, Fitri Yulianti Department of Dermatology and Venereology, Faculty of Medicine, Universitas Padjadjaran - Dr.
Gunawan H, Hidayah RMN, Achdiat PA, Maharani RH, Yulianti F   +4 more
doaj   +3 more sources

Hypohidrotic Ectodermal Dysplasia (ED): A Case Series [PDF]

Journal of Clinical and Diagnostic Research, 2014
Ectodermal Dysplasia (ED) is a rare disorder with defects in two or more of the following structures: the teeth and the skin and its appendages including hair, nails, eccrine, and sebaceous glands.
Mallika Kishore, Sunil R. Panat, Ashish Aggarwal, Nupur Agarwal, Nitin Upadhyay, Kratika Ajai, Abhijeet Alok   +6 more
doaj   +2 more sources

Ectodermal dysplasia - Maxillary and mandibular alveolar reconstruction with dental rehabilitation: A case report and review of the literature

Indian Journal of Plastic Surgery, 2010
Ectodermal dysplasia is a rare group of inherited disorders characterized by aplasia or dysplasia of tissues of ectodermal origin, such as hair, nails, teeth and skin. Dental manifestations include hypodontia, complete anodontia or malformed teeth.
Deshpande Sanjeev, Kumar Vikas
doaj   +4 more sources

SOFT Syndrome: The First Case in Iran

Advanced Biomedical Research, 2018
Primordial dwarfism (PD) is a group of rare genetically heterogeneous disorders consisted of disorders with intrauterine growth retardation continued through the life.
Neda Mostofizadeh, Mahshid Gheidarloo, Mahin Hashemipour, Elham Hashemi Dehkordi   +3 more
doaj   +2 more sources

Do you know this syndrome? Nail patela syndrome: a pathognomonic dermatologic finding [PDF]

Anais Brasileiros de Dermatologia, 2017
: The nail-patella syndrome involves a clinical tetrad of changes in the nails, knees, elbows and the presence of iliac horns. Nail changes are the most constant feature: absent, hypoplastic, or dystrophic.
Bruna Giusto Bunjes, Marcelle da Costa Frickmann Fernandes   +1 more
doaj   +6 more sources

Hereditary Ectodermal Dysplasia in Two Identical Siblings

Acta Medica Bulgarica
Primary defects in two or more ectodermally-derived tissues during embryonic development characterize ectodermal dysplasia, a vast, varied group of inherited illnesses. Skin, hair, nails, eccrine glands, and teeth are the primary tissues affected.
Sarkar A. S., Rao K., Ajila V.
doaj   +2 more sources

Orthodontic Management in Pediatric Patients with Rare Diseases: Case Reports. [PDF]

J Clin Med
Background: The orthodontic management of pediatric patients with rare diseases, such as Ectodermal Dysplasia (ED) and Osteogenesis Imperfecta (OI), requires complex protocols due to dental anomalies in both the number and structure of teeth.
Luzzi V, Fioravanti M, Mitrano L, Marasca B, Saccucci M, Celli M, Celli L, Vozza I, Ierardo G.   +8 more
europepmc   +3 more sources

SYNDROME IN QUESTION [PDF]

Anais Brasileiros de Dermatologia, 2015
The Iso-Kikuchi Syndrome is a rare condition characterized by nail dysplasia involving the index fingers, including micronychia, polyonychia, anonychia, irregular lunula, malalignment and hemionychogryphosis.
Nilton Di Chiacchio, Julio Cesar Jasso-Olivares, Nilton Gioia Di Chiacchio, José Antonio Jacinto, Maria Victoria Suárez Restrepo   +4 more
doaj   +1 more source

Ellis-Van Creveld Syndrome: A Rare Case Report of an Indian Child With Rare Cardiac Anomalies and Normal Intelligence

Cureus, 2022
Ellis-Van Creveld syndrome (EVCS) is an abnormal genetic condition of the EVC2 gene located on chromosome 4. In this case, the person presents with bone growth abnormalities, thus having a short stature, short arms and legs (more commonly the forearm and
Benumadhab Ghosh, Isha Sahai, Gajendra Agrawal, S. Acharya, J. Christopher   +4 more
semanticscholar   +1 more source