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A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

A young man was diagnosed with a rare hair loss condition usually seen in older women.

Trichothiodystrophy is a condition with brittle hair and various physical and mental issues due to low sulfur in proteins.

Lupus affects the body and skin, causing joint pain and skin issues that can be treated with steroids and antimalarial drugs.

A severe medication reaction required long treatment and led to hair loss and thyroid issues.

People with myotonic dystrophy type 1 have a higher chance of getting skin tumors, including melanoma.

A woman with lupus developed rare skin growths that went away on their own.

The study concludes that Loose Anagen Hair Syndrome is a benign condition that usually improves with age but can be hard to diagnose and stressful for the family.

Keratosis Follicularis Spinulosa Decalvans is a rare genetic disorder causing skin and hair issues, often inherited through the X chromosome.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

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

Tissue expansion successfully treated alopecia in a child with hypohidrotic ectodermal dysplasia.

Lupus affects the skin in various ways, and proper skin examination is crucial for diagnosis and treatment.

EFFC might be common but underreported.

The woman has Discoid Lupus Erythematosus and needs specialist care.

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

A rare skin condition was confirmed to be associated with a specific virus in a young girl.

KFSD can be linked to acne keloidalis nuchae and tufted hair folliculitis.

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

Long eyelashes in a patient were an unusual sign of systemic lupus erythematosus.

A patient with a rare hair condition and skin disorder showed hair improvement after treatment.

Treatment with vitamin A did not improve the child's skin condition.

Chronic scarring alopecia is common in SLE patients and needs early detection and management.

A heart transplant patient developed a skin condition called epidermodysplasia verruciformis after taking immune-suppressing drugs.

Two cases of hairy elbows syndrome were described, with normal skin texture and symmetrical hair growth.

The condition is likely inherited in an autosomal-dominant pattern.

Skin symptoms are important for diagnosing and managing juvenile-onset systemic lupus erythematosus and usually get better with treatment.

Hair transplants can rarely cause scalp inflammation leading to hair loss, needing early detection and treatment.