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A patient with Ivemark syndrome developed mixed type vitiligo after a hepatitis C infection, showing different treatment responses and immune cell involvement in the skin.

Brodalumab is more effective than ustekinumab in treating psoriasis.

Cyclophosphamide likely causes skin darkening by affecting hair follicles.

A boy with severe immune deficiency and Epstein-Barr virus died from high-grade B-cell lymphoma.

Early diagnosis and multidisciplinary care, including orthopedic surgery, can prevent long-term disability in IFAP syndrome.

Newborns with the common rash Erythema Toxicum have many active mast cells in their skin, but these cells don't produce the LL-37 peptide.

A 68-year-old woman with benign mucous membrane pemphigoid has eye, mouth, and skin issues, including thick plaques and nail changes.

Early genetic testing and zinc therapy are crucial for managing acrodermatitis enteropathica effectively.

Skin diseases look different on pigmented and nonpigmented skin.

KRT14 gene variants cause dermatopathia pigmentosa reticularis, affecting nails, teeth, and hair.

Woolly hair is a rare genetic condition with no effective treatments.

Pregnancy can cause skin changes and conditions that need correct diagnosis and treatment for the health of the mother and baby.

PRP patients show varied symptoms and need more research to understand related conditions.

A 91-year-old woman's hair turned black in one spot, with skin changes underneath.

Human-induced stem cell-created skin models can help understand skin diseases by studying the skin's layers.

Some children are born with unusually short, fine hair because their hair growth phase is short, but this often gets better by itself during puberty.

Boxer dogs may have a genetic skin condition that worsens seasonally and can be treated with certain medications.

Connexin 30 is usually absent in normal skin but can appear in certain skin conditions.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

A child with Sweet syndrome was found to have chronic granulomatous disease and improved with treatment.

A 20-year-old had hair loss and skin issues from lichen planopilaris starting at age 10.

Patients with myotonic dystrophy often have skin problems that suggest early aging and vitamin D issues, and the severity of these problems is linked to their genetic condition and vitamin D levels.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Mutations in the LIPH gene cause woolly hair in a child.

RPGRIP1L helps skin cells stick together by blocking PKCβII, which can prevent skin blistering like in pemphigus.

A Taiwanese patient had hair loss and skin bumps without the usual gene mutation, suggesting other genetic factors might be involved.