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The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

Cronkhite-Canada syndrome is a rare, non-inherited condition causing various symptoms like polyps, hair loss, and weight loss.

Sleeping on a waterbed caused a skin infection, which cleared up with clindamycin gel.

Some cases of folliculotropic mycosis fungoides may progress slowly and not need aggressive treatment.

A specific gene mutation causes Olmsted syndrome.

DPR can show different hair characteristics, as seen in two brothers with normal hair.

Doctors should actively prevent and treat skin side effects in cancer patients to keep them on the best medication and reduce discomfort.

Dermatopathia pigmentosa reticularis causes skin discoloration, hair loss, and nail problems.

Shaving, erythromycin cream, and clotrimazole powder effectively treated the bad odor and rough hair.

Psoriasis patients have different skin bacteria, which may cause flare-ups.

Papillon-Lefèvre Syndrome causes early tooth loss and skin issues, needing early dental diagnosis.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

Epidermolytic ichthyosis can be inherited in a semidominant way with mild symptoms in carriers.

Two sisters had rare, widespread cysts and complete hair loss, suggesting a genetic link.

C57BL/6 mice and SD rats have different sweat gland and hair follicle patterns, useful for skin research.

Congenital atrichia with papular lesions causes permanent hair loss and skin bumps from birth.

Early diagnosis and treatment of EGFR inhibitor-induced folliculitis decalvans can prevent permanent hair loss.

An adult with a rare skin condition improved with tazarotene treatment.

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.

The newborn's skin blistering is due to a genetic condition called epidermolytic hyperkeratosis.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

A new genetic variant causes BRESHECK syndrome by disrupting cell growth and stress response.

Focal palmoplantar callosities may help diagnose non-Herlitz junctional epidermolysis bullosa.

Mesenchymal stem cells and their vesicles may effectively treat skin diseases, but more research is needed.

Oral retinoic acid effectively treated collodion baby, with hair loss as the main side effect.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

Certain cancer drugs can cause skin issues like rashes and itching.

Lrig1 could be a marker for advanced sebaceous carcinoma.

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

Syphilis can cause hair loss and skin changes in HIV-positive patients, and proper treatment can resolve these symptoms.