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About 3,410 results

ALLMedicine™ Ichthyosis Center

Research & Reviews  1,579 results

Mosaic epidermolytic ichthyosis.
https://doi.org/10.1136/bcr-2020-240424
BMJ Case Reports; Mendes SR, Gameiro AR et. al.

Feb 19th, 2021 - Mosaic epidermolytic ichthyosis.|2021|Mendes SR,Gameiro AR,Cardoso JC,Reis JP,|

Unbound Corneocyte Lipid Envelopes in 12R-Lipoxygenase Deficiency Support A Specific Ro...
https://doi.org/10.1016/j.ajpath.2021.02.005
The American Journal of Pathology; Meyer JM, Crumrine D et. al.

Feb 19th, 2021 - Loss-of-function mutations in arachidonate lipoxygenase 12B (ALOX12B) are an important cause of autosomal recessive congenital ichthyosis (ARCI). 12R-lipoxygenase (12R-LOX), the protein product of ALOX12B, has been proposed to covalently bind the ...

Acquired ichthyosis and false-positive hepatitis A serology as paraneoplastic phenomena...
https://doi.org/10.1136/bcr-2020-240966
BMJ Case Reports; Phillips AL, Parmar SC et. al.

Feb 18th, 2021 - Acquired ichthyosis and false-positive hepatitis A serology as paraneoplastic phenomena in anaplastic lymphoma kinase-positive anaplastic large-cell lymphoma.|2021|Phillips AL,Parmar SC,Yakubu UK,Chin MF,|

Epidermolytic epidermal nevus caused by a somatic mutation in KRT2.
https://doi.org/10.1111/pde.14529
Pediatric Dermatology; Mohamad J, Samuelov L et. al.

Feb 8th, 2021 - Superficial epidermolytic ichthyosis (formerly Ichthyosis bullosa of Siemens) is an uncommon condition caused by dominant mutations in KRT2 encoding keratin 2. Epidermolytic epidermal nevus due to somatic mutations in KRT2 is even rarer. Here, we ...

Filaggrin expression via immunohistochemistry in basal cell carcinoma and squamous cell...
https://doi.org/10.1111/cup.13975
Journal of Cutaneous Pathology; Vanderbeck K, Orr CE et. al.

Feb 5th, 2021 - Filaggrin is a protein integral to the structure and function of the epidermis. Filaggrin (FLG) loss-of-function (LOF) mutations are common and increase the risk of developing atopic dermatitis (AD) and ichthyosis vulgaris (IV). Epidemiologic data...

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Guidelines  1 results

Management of congenital ichthyoses: European guidelines of care, part two.
https://doi.org/10.1111/bjd.16882
The British Journal of Dermatology; Mazereeuw-Hautier J, Hernández-Martín A et. al.

Jun 13th, 2018 - These guidelines for the management of congenital ichthyoses have been developed by a multidisciplinary group of European experts following a systematic review of the current literature, an expert conference held in Toulouse in 2016, and a consens...

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Drugs  83 results see all →

Clinicaltrials.gov  1,693 results

Mosaic epidermolytic ichthyosis.
https://doi.org/10.1136/bcr-2020-240424
BMJ Case Reports; Mendes SR, Gameiro AR et. al.

Feb 19th, 2021 - Mosaic epidermolytic ichthyosis.|2021|Mendes SR,Gameiro AR,Cardoso JC,Reis JP,|

Unbound Corneocyte Lipid Envelopes in 12R-Lipoxygenase Deficiency Support A Specific Ro...
https://doi.org/10.1016/j.ajpath.2021.02.005
The American Journal of Pathology; Meyer JM, Crumrine D et. al.

Feb 19th, 2021 - Loss-of-function mutations in arachidonate lipoxygenase 12B (ALOX12B) are an important cause of autosomal recessive congenital ichthyosis (ARCI). 12R-lipoxygenase (12R-LOX), the protein product of ALOX12B, has been proposed to covalently bind the ...

Acquired ichthyosis and false-positive hepatitis A serology as paraneoplastic phenomena...
https://doi.org/10.1136/bcr-2020-240966
BMJ Case Reports; Phillips AL, Parmar SC et. al.

Feb 18th, 2021 - Acquired ichthyosis and false-positive hepatitis A serology as paraneoplastic phenomena in anaplastic lymphoma kinase-positive anaplastic large-cell lymphoma.|2021|Phillips AL,Parmar SC,Yakubu UK,Chin MF,|

Epidermolytic epidermal nevus caused by a somatic mutation in KRT2.
https://doi.org/10.1111/pde.14529
Pediatric Dermatology; Mohamad J, Samuelov L et. al.

Feb 8th, 2021 - Superficial epidermolytic ichthyosis (formerly Ichthyosis bullosa of Siemens) is an uncommon condition caused by dominant mutations in KRT2 encoding keratin 2. Epidermolytic epidermal nevus due to somatic mutations in KRT2 is even rarer. Here, we ...

Filaggrin expression via immunohistochemistry in basal cell carcinoma and squamous cell...
https://doi.org/10.1111/cup.13975
Journal of Cutaneous Pathology; Vanderbeck K, Orr CE et. al.

Feb 5th, 2021 - Filaggrin is a protein integral to the structure and function of the epidermis. Filaggrin (FLG) loss-of-function (LOF) mutations are common and increase the risk of developing atopic dermatitis (AD) and ichthyosis vulgaris (IV). Epidemiologic data...

see more →

News  41 results

Consensus Statement Issued on Retinoids for Ichthyosis, Disorders of Cornification
https://www.medscape.com/viewarticle/945212

Feb 2nd, 2021 - Clinicians using systemic retinoids for treating ichthyosis and other disorders of cornification (DOC) in children and adolescents should aim for the lowest dose possible to balance therapeutic goals with acceptable toxicity levels, advised the au...

Chronic Diarrhea in an Adolescent Girl With a Genetic Skin Condition
https://www.mdedge.com/dermatology/article/217738/rare-diseases/chronic-diarrhea-adolescent-girl-genetic-skin-condition?channel=113
Lucia Liao, BS, Andrea Zaenglein, MD et. al.

Feb 24th, 2020 - The Diagnosis: Netherton Syndrome Netherton syndrome (NS) is a rare autosomal-recessive disorder characterized by a clinical triad of ichthyosis linearis circumflexa; atopic diathesis; and hair shaft abnormalities, most classically trichorrhexis i.

Seborrhea Herpeticum: Cutaneous Herpes Simplex Virus Infection Within Infantile Seborrheic Dermatitis
https://www.mdedge.com/dermatology/article/211565/pediatrics/seborrhea-herpeticum-cutaneous-herpes-simplex-virus-infection?channel=45
Laryn Steadman, MD, Katherine Hrynewycz, MD et. al.

Nov 5th, 2019 - Classically, eczema herpeticum is associated with atopic dermatitis (AD), but it also has been previously reported in the setting of pemphigus vulgaris, Darier disease, ichthyosis vulgaris, burns, psoriasis, and irritant contact dermatitis. 1,2 Des.

Make the diagnosis
https://www.mdedge.com/pediatrics/article/196680/pediatrics/make-diagnosis
Donna Bilu Martin, MD

Mar 20th, 2019 - Ichthyosis vulgaris Ichthyoses describe a group of disorders of cornification in which the epidermis differentiates abnormally, leading to generalized scaling of the skin. Ichthyosis is derived from the Greek word for fish, “ichthys.

A 13-month-old, healthy black male presented with a 6-month history of dry, scaly skin on the body
https://www.mdedge.com/dermatology/article/196680/pediatrics/13-month-old-healthy-black-male-presented-6-month-history-dry?channel=39212
Donna Bilu Martin, MD

Mar 20th, 2019 - Ichthyosis vulgaris Ichthyoses describe a group of disorders of cornification in which the epidermis differentiates abnormally, leading to generalized scaling of the skin. Ichthyosis is derived from the Greek word for fish, “ichthys.

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Patient Education  13 results see all →