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Using cidofovir cream for a rare skin disease can cause skin darkening.

DEC cells show promise as a safe and effective treatment for Duchenne muscular dystrophy.

Cronkhite-Canada syndrome is a rare condition causing gut polyps, hair loss, skin changes, and nail issues, often with a poor outlook.

Mutant CDP/Cux protein causes hair defects and reduced male fertility in mice.

Removing Ctip2 in skin cells causes skin inflammation similar to atopic dermatitis.

Inhibiting ornithine decarboxylase may help prevent certain skin cancers.

ICD codes for skin conditions vary in accuracy, needing better validation for some common conditions.

Mutant Cx43 causes slower wound healing and hair growth issues in ODDD.

A 56-year-old man was diagnosed with Cronkhite-Canada Syndrome after showing symptoms like diarrhea, weight loss, and skin changes.

scMC effectively separates biological signals from technical noise in single-cell genomics data.

Mice with a mutated Dsg3 gene showed severe symptoms but not the typical blistering of pemphigus vulgaris.

Fibroblast changes in systemic sclerosis may help understand disease severity and treatment.

Cholecystokinin may help reduce skin inflammation in psoriasis.

A girl with a rare skin condition improved after one month of treatment with acitretin.

A new mutation in the STS gene causes X-linked ichthyosis, even in rare female cases.

A woman with X-linked chronic granulomatous disease developed lupus-like skin lesions, improved with treatment, suggesting a unique skin condition in carriers.

A new genetic mutation causing Xeroderma Pigmentosum was found in an 8-year-old girl, affecting her DNA repair.

Zinc supplements improved the girl's skin and hair condition.

Antiviral drugs, especially daclatasvir, may be a new treatment for a rare skin disease, improving survival and reducing symptoms in mice.

A Shih Tzu with Cushing syndrome developed skin issues and was euthanized after treatment led to neurological problems.

Non-drug methods effectively managed agitation in a patient with a heart device, leading to improved mental function.

Early genetic testing and new therapies like secukinumab are crucial for managing Netherton syndrome effectively.

Deleting Snai2 and Snai3 causes fatal autoimmunity.

Molluscum contagiosum can occur in epidermoid cysts, especially with prolonged steroid use.

A woman developed severe bladder inflammation after cancer treatment with Cytoxan.

A new one-step test can quickly identify skin cancer during surgery.

A cancer patient's hair became permanently curly after treatment with nivolumab.

People with mycosis fungoides/Sézary syndrome have a much lower quality of life.