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A new mutation in the TRPS1 gene caused Trichorhinophalangeal syndrome in a 17-year-old, highlighting the need for genetic testing.

Tissue-engineered skin substitutes can model junctional epidermolysis bullosa and may help develop gene therapy.

Steroid sulfatase inhibitors could help treat hormone-related disorders and cancers.

Women's hair has more sulfur, and black hair has more calcium than white hair.

Early diagnosis and treatment of TPP can prevent complications.

A 21-month-old boy has a rare genetic disorder causing sparse hair due to an LSS gene mutation.

LHTric-1 is a specific antibody useful for studying hair and nail formation.

Radiological findings help distinguish LAM, PLCH, and BHD to avoid invasive tests.

Thymoma-associated multiorgan autoimmunity can cause liver damage and affects multiple organs, with limited treatment options and a generally poor prognosis.

Natural hair reflects identity and history, while modifications signal social pressures.

The sensor accurately measures thallium ions in solutions with high selectivity.

OCT can effectively examine and reveal details about human hair and scalp conditions.

Rectangular black granules, solitary yellow dots, and mostly single-hair follicles suggest Loose Anagen Hair Syndrome.

Trichoscopy is good for telling apart tinea capitis and alopecia areata in kids.

A genetic mutation in the LIPH gene causes a rare hair disorder with sparse, curly hair.

Trichodysplasia spinulosa is a rare skin disease in immunocompromised patients caused by a specific virus targeting hair follicle cells.

CTHRC1 helps sweat glands recover by rebuilding nearby blood vessels.

If a child is losing a lot of eyelashes and it keeps happening, doctors should look carefully at their health history because it might be a sign of a different health problem.

Hair shaft changes may be linked to CCCA, but their role is unclear.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

An 11-year-old girl with compulsive hair pulling was successfully treated with therapy and medication.

BBS7 is crucial for healthy gums and teeth by supporting cell and blood vessel function.

A new TP63 mutation was found in a baby with EEC syndrome, showing the need for TREC testing to check for immune issues.

A defective gene causes hair loss and taste insensitivity in BTBR mice.

The SHJH hr mice with a mutated Hr gene show signs of faster skin aging due to poor antioxidative protection.

Toxic Shock Syndrome progresses quickly, often involves multiple organs, and is linked to Staphylococcus aureus toxins, with treatment options available but diagnostic challenges remaining.

Thymic mesenchymal cells have unique gene expression that supports their specific functions in the thymus.

CDH3-related disease causes worsening eye and hair issues.

The Aqualon SLT device measures hair stiffness and slipperiness to evaluate hair treatments.