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Clouston Syndrome: 25-year follow-up of a patient [PDF]

Anais Brasileiros de Dermatologia, 2015
: Clouston syndrome is a rare genodermatosis that affects skin and annexes. It is a form of ectodermal dysplasia characterized by generalized hypotrichosis, palmoplantar hyperkeratosis and nail dystrophy.
Lívia Arroyo Trídico, João Roberto Antonio, Eurides Maria de Oliveira Pozetti, Ana Maria Mendes Rosa, Carlos Roberto Antonio   +4 more
doaj   +12 more sources

Clouston Syndrome: Report of a Jordanian Family with GJB6 Gene Mutation [PDF]

Case Reports in Dermatological Medicine, 2023
Ectodermal dysplasias (ED) encompass a collection of conditions wherein the development of two or more structures derived from the ectoderm exhibits abnormal patterns.
Rand Murshidi, Heba Al-lala
doaj   +8 more sources

Do you know this syndrome? Clouston syndrome [PDF]

Anais Brasileiros de Dermatologia, 2017
Ectodermal dysplasias are conditions that present primary defects in two or more tissues of ectodermal origin and can be classified as hypohidrotic and hidrotic.
Sarah Sanches, Priscila Regina Orso Rebellato, Andréa Buosi Fabre, Giovana Liz Marioto de Campos   +3 more
doaj   +10 more sources

Mutation–proved Clouston syndrome in a large Indian family with a variant phenotype [PDF]

Indian Journal of Dermatology, 2019
Hereditary ectodermal dysplasias, a group of disorders affecting skin, hair, nails, and teeth, consist of two main clinical forms – hypohidrotic and hidrotic.
Sangeeta Khatter, Ratna Dua Puri, Sunita Bijarnia Mahay, Pratibha Bhai, Renu Saxena, Ishwar C Verma   +5 more
doaj   +6 more sources

Palmar syringofibroadenoma-like lesions in Clouston syndrome treated with CO2 ablative laser [PDF]

JAAD Case Reports, 2023
Meryem Safoine, MD, PhD, Danielle Bouffard, MD, Elena Netchiporouk, MD, MSc, Catherine Maari, MD   +3 more
doaj   +8 more sources

Clouston syndrome with palmoplantar keratoderma

Journal of Indian Academy of Oral Medicine and Radiology, 2011
Clouston syndrome (hidrotic ectodermal dysplasia) is characterized by the clinical triad of nail dystrophy, alopecia and palmoplantar hyperkeratosis. Clouston syndrome is transmitted as an autosomal dominant trait and caused by mutations in the GJB6 gene
M P Singh, Manishi Singh, Manika Singh, Prashant Tripathi   +3 more
doaj   +4 more sources

Clouston Syndrome: First Case in Russia [PDF]

Balkan Journal of Medical Genetics, 2012
Clouston Syndrome: First Case in RussiaHidrotic ectodermal dysplasia type 2 (HED2) or Clouston syndrome (OMIM #129500) is a rare autosomal dominant genetic disorder which affects skin and its derivatives, characterized by the major triad of features: nail dystrophy, generalized hypotrichosis, and palmoplantar hyperkeratosis.
Marakhonov A, Skoblov M, Galkina V, Zinchenko R   +3 more
doaj   +6 more sources

Clouston syndrome associated with eccrine syringofibroadenoma [PDF]

Anais Brasileiros de Dermatologia, 2014
Eccrine syringofibroadenoma is a rare benign neoplasia derived from acrosyryngium cells of the eccrine sudoriferous glands. It affects the extremities of elderly individuals as solitary tumors, or may also present as multiple lesions.
Ana Carolina Dias Viana de Andrade, Denise Cardoso Vieira, Olga Maria Oiticica Harris, Matheus Melo Pithon   +3 more
doaj   +7 more sources

Connexin hemichannel inhibition improves skin pathology in Clouston syndrome mice [PDF]

EBioMedicine, 2020
Roberto Bruzzone, Thomas W. White
doaj   +5 more sources

When Rare Meets Risky: Clouston Syndrome with Cutaneous Squamous Cell Carcinoma [PDF]

Indian Dermatology Online Journal
Satyendra K. Singh, Atul Mohan, Bhagirath Bhakar, Soumya Bansal   +3 more
doaj   +5 more sources