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Modern techniques improve scalp reconstruction after trauma.

A man developed skin cancer on his scalp after multiple artificial hair grafts.

A child with skin and heart issues had rare genetic mutations affecting skin and heart cell cohesion.

A woman with a rare hair loss condition developed skin cancer in the bald area.

A rare fungal infection on a child's scalp was successfully treated with antifungal medication.

Baldness is common in Korean men (60.5%), and those with a family history are 3.1 times more likely to have hairline recession.

Chronic scalp inflammation can turn into cancer, so regular check-ups are important.

Epidermoid cysts can be better diagnosed with ultrasound by recognizing specific features and using clinical information.

Early diagnosis and treatment of hair and scalp diseases in children can improve their growth and mental health.

In a Tuscan pediatric clinic, 7.19% of children had hair or scalp disorders, with nonscarring alopecia being the most common.

An infant with complete hair loss was diagnosed with a genetic disorder affecting hair growth.

Early diagnosis and genetic evaluation of ADULT syndrome are crucial to reduce stress and medical costs.

A 12-year-old girl was misdiagnosed with alopecia areata but actually had a nevus sebaceus with a genetic mutation.

Melanocytic matricoma can look like skin cancer but is usually harmless; surgery and follow-up are advised.

A baby with KID syndrome died from infections and organ failure at 18 months old.

Children with Parry Romberg Syndrome had successful facial fat-grafting surgeries after disease stabilization with no complications.

A young man was unexpectedly diagnosed with basal cell carcinoma after a scalp examination and confocal microscopy.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Scalp reduction can improve hair distribution in certain baldness cases but requires careful patient selection and understanding of facial structure.

The hair defect is due to abnormal inner root sheath keratinization.

Square-shaped hair loss can occur after treating a brain aneurysm due to localized radiation exposure.

KID syndrome should be reclassified as an ectodermal dysplasia.

The Sacred Heart Bilobed Flap is a surgical method for repairing small scalp defects with local flaps, relying on scalp elasticity and hair regrowth to hide any imperfections.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

A man with hair loss and a scalp lump was diagnosed with a diffuse neurofibroma but chose not to have surgery.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

An infant with scalp fungus was cured after extended treatment with antifungal medication.

Shrunken heads retain some facial features and hair characteristics, allowing for limited individual identification.

Tissue expanders effectively repair large scalp defects and restore a natural-looking scalp.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.