Results 11 to 20 of about 1,415 (230)
Pigment International, 2018 The term “acral” means the distal portions of the limbs (hand, foot) and the head (ears, nose). The term acral melanosis is loosely applied to an increase in melanin pigmentation, in a diffuse, reticulate, or focal pattern over the distal parts of the ...
Mala Bhalla, Shimona Garg
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Dowling Degos Disease in a child: A rare case report from Northeast India
Indian Journal of Paediatric Dermatology, 2021 Dowling–Degos disease (DDD) is a rare genodermatosis with autosomal dominant inheritance. It is characterized by reticulate pigmentation of flexures, comedo-like follicular papules, and perioral pitted scars.
Romita Bachaspatimayum +2 more
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Pigment International, 2021 Background: Lichen planus (LP) is a papulosquamous skin disorder characterized by violaceous polygonal papules and plaques associated with itching.
Ashiwini S Tatawati +2 more
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Dermoscopy in Vitiligo: An emerging armamentarium in diagnosis and activity assessment
Pigment International, 2022 Context: Vitiligo is an autoimmune depigmentary disorder characterized by loss of epidermal melanocytes. It can be diagnosed clinically, however, dermoscopy aids in its differentiation from other hypopigmentary and depigmentary conditions and also helps ...
Guneet Awal +2 more
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Clinical and Genetic Review of Hereditary Acral Reticulate Pigmentary Disorders
Dermatology Research and Practice, 2017 Reticulated pigmentation is a unique pigmentary change caused by a heterogeneous group of hereditary and acquired disorders. This pigmentation is characterized by a mottled appearance, with lesions that vary in size and pigmentary content.
H. Alshaikh, F. Alsaif, S. Aldukhi
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Indian Journal of Dermatology, 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 Galli ...
Biju Vasudevan +5 more
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Naegeli–Franceschetti–Jadassohn syndrome: A rare reticulate pigmentary disorder
Indian Journal of Dermatology, 2019 Naegeli–Franceschetti–Jadassohn syndrome is a rare autosomal dominant form of ectodermal dysplasia affecting sweat glands, nails, teeth, and skin. We report a case of 16-year-old female who had generalized reticulate pigmentation, dental changes, nail ...
Gitika Sanodia +2 more
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Reticulate dyschromia, congenital atrichia and speech delay in a child: A diagnostic dilemma
Indian Journal of Paediatric Dermatology, 2018 Disorders of reticulate dyschromia can be diagnosed on the basis of the distribution and type of pigmentation in association with coexisting abnormalities.
Tasleem Arif +2 more
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A case of dyschromatosis universalis hereditaria with adermatoglyphia: A rare association
Indian Dermatology Online Journal, 2015 Dyschromatosis universalis hereditaria (DUH) is a rare, autosomal dominant genodermatosis with a peculiar reticulate pigmentary change, consisting of hyperpigmented macules mingled with hypopigmented lesions to give an overall impression of mottling.
Sumir Kumar +2 more
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Dermatopathia pigmentosa reticularis: A rare case report and review of literature
Clinical Dermatology Review, 2022 Dermatopathia pigmentosa reticularis is a rare autosomal dominant disorder. It is an ectodermal dysplasia, characterized by a triad of generalized reticulate hyperpigmentation, noncicatricial alopecia, and onychodystrophy.
Aswath Rajan +4 more
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