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

A direct brow lift can effectively fix nerve damage and improve appearance after surgery.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

Using a person's own fat cells can help regrow hair after injury.

Topical tacrolimus can effectively treat erosive pustular dermatosis and related hair loss.

Deleting NIPP1 in mouse skin cells causes early aging and chronic skin issues.

Mitochondriopathy may cause eyelash loss.

Fat tissue transplant may be an effective new treatment for severe, treatment-resistant hair loss from folliculitis decalvans.

A woman's hair loss was initially mistaken for a common hair loss condition but was later found to be caused by breast cancer cells in her scalp.

Metastatic cervical cancer can cause rare, severe Cushing's syndrome with high risk of death.

A man with a rare adrenal cancer showed unusual symptoms and died four months after diagnosis.

Nevus comedonicus is a rare skin condition with grouped open pores, sometimes linked to other body issues.

Early biopsy is crucial for diagnosing rare skin sarcoidosis, improving treatment.

Eyelash transplantation can cause eye damage and pain if not done carefully.

Deleting Smad4 and PTEN genes in mice causes rapid, invasive stomach cancer.

Naevoid bundle hair is an unusual hair growth pattern where multiple hairs fuse together.

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

A super thin DIEP flap can effectively reconstruct scalp defects with good skin coverage and contour.

The rib-sparing technique in breast reconstruction may lead to more complications without reducing the need for further surgery.

Trichoscopy can diagnose Netherton syndrome without pulling hairs.

An American Bully with a genetic skin condition improved significantly with specific topical treatments.

Astrotactin-2 is cleaved in a specific way that helps understand its maturation.

Using combined hair restoration methods can effectively treat severe scalp wrinkling.

The procedure effectively improved facial appearance with high satisfaction and low complications.

The calcineurin/NFAT pathway plays a significant role in the development and growth of a type of skin cancer called cutaneous squamous cell carcinoma.

Congenital Triangular Alopecia is a rare, non-scarring hair loss that can be surgically treated in females for cosmetic reasons.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.