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The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

Double pulse dose terbinafine effectively treats kerion type of tinea capitis.

The p.P25L mutation in the KRT5 gene causes a rare skin condition that worsens over time and may lead to hair loss starting in young adulthood.

Temporal triangular alopecia is a lifelong condition with hairless patches on the side of the head that may be present from birth.

Two siblings have a rare hair condition caused by a new genetic variant.

Scalp itching can be caused by various skin conditions, hair loss, allergies, or anxiety.

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

A 2-year-old boy was diagnosed with a rare genetic condition causing fragile hair, intellectual issues, and short stature.

A 2-year-old boy has a rare hair disorder causing brittle hair and hair loss, which may improve with age.

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

Persistent papular plaques on children's faces need better understanding and treatment.

A new syndrome may link skin, growth, mental, and hair issues.

Emotional factors are crucial in treating and preventing scalp neurodermatitis and hair loss.

A baby from an Indian family had a rare genetic disorder causing no scalp or body hair due to a specific gene deletion.

The guide explains how to identify and treat children's hair loss, including fungal infections, autoimmune disorders, hairstyle changes, self-correcting conditions, and behavioral therapy for hair-pulling.

A rare skin condition affected only the facial hair of a 46-year-old man.

Keratosis pilaris causes small skin bumps, mainly in women, and treatments offer only temporary relief.

Small white dots on the scalp seen with a dermoscope correspond to sweat ducts and vary with different hair disorders.

An 11-year-old girl's hair loss was caused by a Cladosporium fungal infection, which was cured with itraconazole treatment.

Monilethrix is a genetic hair disorder causing fragile, beaded hair with no effective treatment.

Mutations in the LSS gene cause hair loss and may affect brain development, with varying severity.

Trichoscopy is a useful, painless tool for diagnosing and monitoring children's hair and scalp issues.

The girl has a genetic hair condition causing thin hair since childhood.

Early diagnosis and treatment of Lichen Planopilaris are crucial to prevent permanent hair loss.

A new genetic mutation was found causing hair and eye issues in a boy.

A rare hair follicle disorder can cause itchy, bluish-black bumps on the body.

Alopecia areata and lichen planus can occur together in children, which is important for diagnosis and treatment.

A woman had a rare infection of both white piedra and head lice, which improved after 10 weeks of antifungal treatment.

A 12-year-old boy has a rare, harmless hair loss on his chin with no need for treatment.

Pseudopelade of Brocq is a unique hair loss condition, but its cause and development are still not fully understood.