Zobrazeno 1 - 10 of 88 pro vyhledávání: '"Reticulate acropigmentation of Kitamura"'
1
Akademický článek
Dowling–Degos disease with reticulate acropigmentation of Kitamura: Extended spectrum of a single entity
Autor: Shyam Govind Rathoriya, Sumit S. L Soni, Dinesh Asati
Publikováno v: Indian Dermatology Online Journal, Vol 7, Iss 1, Pp 32-35 (2016)
Dowling–Degos disease (DDD) and reticulate acropigmentation of Kitamura (RAK) are rare genodermatoses inherited as an autosomal dominant trait with variable penetrance. They are considered to be part of a spectrum of reticulate pigmentary dermatose
Externí odkaz: https://doaj.org/article/b7008cfb70664c5d987bedb6098e3eb8
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2
Akademický článek
A rare case of late onset reticulate acropigmentation of Kitamura without involvement of the palms and soles
Autor: Conny Melly, Vini Onmaya, Sri Adi Sularsito, Sondang Panjaitan Sirait, Rahadi Rihatmadja, Indah Widyasari
Publikováno v: JDVI (Journal of General Procedural Dermatology & Venereology Indonesia), Vol 1, Iss 1, Pp 25-28 (2015)
Background: Reticulate acropigmentations of Kitamura (RAPK) is an autosomal dominant inherited disorder characterized by pigmented, angulated, irregular freckle-like lesion with atrophy on the surface, arranged in a reticulate pattern on the dorsa of
Externí odkaz: https://doaj.org/article/5dc98ba2f2fa48f3ad539ef13fddc829
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3
Akademický článek
Acropigmentation of Kitamura with immigration delay disease: A rare entity
Autor: Sumir Kumar, Bharat Bhushan Mahajan, Nidhi Kamra, Pritish A Bhoyar
Publikováno v: Indian Dermatology Online Journal, Vol 6, Iss 3, Pp 210-212 (2015)
Reticulate acropigmentation of Kitamura (RAK) is a rare, autosomal dominant disorder first described in Japan characterised by a reticulate pattern of slightly atrophic, angulated, hyperpigmented macules affecting the acral areas of the body. We here
Externí odkaz: https://doaj.org/article/0ca19904f62d49439f595ca0491b9d9b
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5
Akademický článek
A case of reticulate acropigmentation of Kitamura: Dowling Degos disease overlap with unusual clinical manifestations
Autor: Biju Vasudevan, Rajesh Verma, Sonia Badwal, Vijendran Pragasam, Nikhil Moorchung, Ambresh Badad
Publikováno v: Indian Journal of Dermatology, Vol 59, Iss 3, Pp 290-292 (2014)
Reticulate hyperpigmentary disorders are a group of rare genetic pigmentary abnormalities which includes reticulate acropigmentation of Kitamura (RAPK), Dowling-Degos disease (DD), reticulate acropigmentation of Dohi (RAPD), Haber′s syndrome, and G
Externí odkaz: https://doaj.org/article/8e99a7afb90c4c71b612786914fb5ad2
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8
Akademický článek
Coexistence of reticulate acropigmentation of Kitamura and Dowling-Degos disease
Autor: Ana Rita Cabral, Felicidade Santiago, José Pedro Reis
Publikováno v: Dermatology Reports, Vol 3, Iss 2, Pp e33-e33 (2011)
Reticulate acropigmentation of Kitamura (RAK) and Dowling-Degos Disease (DDD) are rare genodermatosis inherited as an autosomal dominant trait with variable penetrance. They are part of a spectrum of diseases with hyperpigmented macules coalescing in
Externí odkaz: https://doaj.org/article/e1a7b0001d47454e981d1bc34933672a
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10
A Female with Freckles Like Pigmentation on Face and Extremities
Autor: Kananbala Sahu, Swetalina Pradhan
Publikováno v: Clinical Cases in Disorders of Melanocytes ISBN: 9783030227562
Reticulate acropigmentation of Kitamura is an autosomal dominant condition with an onset in first to second decade of life. A 24-year-old female presented with pigmentation over face and hands since her adolescent age. Another notable finding bilater
Externí odkaz: https://explore.openaire.eu/search/publication?articleId=doi_________::2aee35d6c9b87acaaaddfb3e992087fb
https://doi.org/10.1007/978-3-030-22757-9_21
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