Results 11 to 20 of about 836 (156)

Lipoid proteinosis: A rare case revisited

open access: yesIndian Journal of Dermatology, 2023
Arun Achar   +5 more
doaj   +4 more sources

Lipoid proteinosis

open access: yesIndian Journal of Dermatology, 2006
A three and half years old female child with lipoid proteinosis with no history of parental consanguinity and affected siblings has been reported here.
Mukhija Pooja   +3 more
doaj   +4 more sources

Lipoid Proteinosis. [PDF]

open access: yesInt J Clin Pediatr Dent, 2016
Lipoid proteinosis (LP) is an uncommon, autosomal, recessively inherited disorder. It is typically characterized by hoarseness from early infancy, together with various cutaneous manifestations such as waxy papules, acneiform scarring, and eyelid beading.
Mittal HC, Yadav S, Malik S, Singh G.
europepmc   +7 more sources

Lipoid proteinosis: Review of Indian cases. [PDF]

open access: yesJ Oral Maxillofac Pathol, 2022
Lipoid proteinosis (LP) is a rare autosomal recessive disorder characterized by the deposition of amorphous hyaline material in the dermis and submucosal connective tissue. To date <500 cases of LP have been described and oral manifestations described in a very few reports.
Shah JS, Shah HA.
europepmc   +3 more sources

Lipoid proteinosis coexisting with rare psychiatric manifestations: a case report with a review of literature

open access: yesPrzegląd Dermatologiczny, 2023
Lipoid proteinosis is a rare autosomal recessive genodermatosis characterized by the deposition of hyaline material in the skin and internal organs. Skin involvement is in the form of blisters in infancy healing with pock-like scars, yellow waxy papules,
Kritika Gupta   +5 more
doaj   +1 more source

Successful use of acitretin in an indian child with lipoid proteinosis

open access: yesIndian Journal of Paediatric Dermatology, 2022
Introduction: Lipoid proteinosis is a rare autosomal recessive disease, characterized by deposition of Periodic Acid‒Schiff-positive hyaline material in the skin, mucous membrane of the upper aerodigestive tract, and different organs of the body ...
Shraddha P Kote   +3 more
doaj   +1 more source

Lipoid proteinosis: Curious case of two siblings! [PDF]

open access: yesIndian Dermatology Online Journal, 2020
Pooja Agarwal   +3 more
doaj   +2 more sources

Lipoid proteinosis: Unfamiliar skin findings delay diagnosis [PDF]

open access: yesJAAD Case Reports, 2018
Robert E Watson   +2 more
exaly   +2 more sources

A Rare Genodermatosis: Lipoid Proteinosis

open access: yesCerrahpaşa Medical Journal, 2021
Lipoid proteinosis is a rare genodermatosis that manifests with hoarseness and cutaneous findings. Its skin manifestations start with vesicles during the neonatal period, later scar formation and lichenification are observed.
Defne Özkoca   +3 more
doaj   +1 more source

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