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A six-year-old boy with excessive hair growth and other symptoms may have a genetic link on chromosome 17q, requiring regular medical follow-ups.

Erosive pustular dermatosis of the scalp causes painful, scarring skin lesions on the scalp, mainly in elderly people with sun-damaged skin.

The skin condition Ulerythema ophryogenes did not improve with treatment in a patient with other birth defects.

A new mouse mutation causes skin and hair defects due to a gene change.

Frontal Fibrosing Alopecia is a hair loss condition mainly affecting postmenopausal women, with unclear causes and various clinical patterns.

CCCA affects adolescents too, with genetic and environmental links, requiring careful diagnosis.

The patient's scalp lesions stabilized with a combination of treatments after initial therapies failed.

Dermatoscopy helps diagnose hair and scalp disorders in people with Afro-textured hair, but more research is needed for better understanding and treatment.

EPDS can cause recurring scalp sores and hair loss if not treated.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

Accurate diagnosis of APL is crucial to avoid unnecessary treatments.

Local flaps are effective for covering small to large scalp and forehead defects with good cosmetic results.

Researchers found that dissecting folliculitis of the scalp is linked to obesity, severity increases with duration and number of nodules, and early treatment is important to prevent scarring.

A baby boy with 13q deletion syndrome had eye cancer, a woman's vision improved after stopping a breast cancer drug, a man developed cataracts from using Propecia, and a rare skin disorder called Lipoid Proteinosis was discussed. Also, a tool called OCT is useful for diagnosing macular diseases.

A man with Cronkhite-Canada syndrome had all 20 nails detach but improved with treatment.

The patient likely has Chrousos syndrome, a rare condition causing insensitivity to glucocorticoids, requiring high-dose dexamethasone treatment.

Frontal fibrosing alopecia is increasing, especially in postmenopausal women, and treatment with finasteride can improve it.

Rubbing or pressing on the face can cause small bumps, and changing posture along with certain creams can improve them.

A rare scalp condition was successfully treated with specific medications after 9 months.

Frontal fibrosing alopecia in men is often misdiagnosed and needs better diagnostic criteria and treatments.

A 5-year-old girl has sparse, dry, and brittle hair but is otherwise healthy.

Endoscopy-assisted surgery for craniosynostosis showed excellent outcomes with minimal complications and most patients went home the day after surgery.

Patients with skin disorders face higher risks of complications in facial cosmetic surgery.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

A heterozygous mutation in HTRA1 can cause severe CARASIL symptoms.

CCCA is a common, progressive hair loss condition that may not always be linked to hair care practices and requires a biopsy for diagnosis.

Mostly postmenopausal Caucasian women get Frontal Fibrosing Alopecia, which often includes eyebrow loss and has limited treatment success.

A new genetic change in the keratin 10 gene caused a skin condition called ichthyosis hystrix in a father and his daughter.