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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.

A 6-year-old girl had both monilethrix and trichorrhexis nodosa, causing brittle hair, with minimal improvement from treatment.

Corkscrew hair may be a new sign for quickly diagnosing scalp fungus in black children.

A rare cataract surgery complication was successfully treated with laser capsulotomy.

Hidradenitis Suppurativa is a chronic skin condition best treated early with surgery for better outcomes and less recurrence.

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.

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

Inhaled steroids in children may cause excessive hair growth and not always go away after stopping the medication.

Tinea capitis is a fungal infection of the scalp that mainly affects children and can cause symptoms from mild itching to severe inflammation.

Trichothiodystrophy involves brittle hair due to low sulfur amino acids, not a transport defect.

A Turkish woman has a hair condition caused by a LIPH gene mutation.

A boy's growth and immune problems were caused by a new mutation in the STAT5B gene.

Ankle braces reduce motion, while external focus improves hip and knee movements.

Trichotillomania is a chronic hair-pulling disorder that starts in early teens and causes distress and hair loss.

Tofacitinib effectively treated a woman's complex autoimmune and autoinflammatory disorders.

Hair thinning and loss in a girl with a rare metabolic disorder was linked to her condition.

Hair shaft malformation contributes to Central Centrifugal Cicatricial Alopecia.

Hair loss improved with treatment and successful transplant.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

Trichostasis spinulosa can be diagnosed with a simple skin biopsy and treated with specific gels, but lesions may return after stopping treatment.

A 17-year-old boy with Temporal Triangular Alopecia successfully grew new hair after a hair restoration surgery using follicular unit transplantation.

A 12-year-old girl was diagnosed with monilethrix, a genetic condition causing fragile, beaded hair that breaks easily, with no effective treatment available.

The man had myotonia, which caused delayed hand grip relaxation.

TNF-a may not be as involved in certain types of hair loss as previously thought.

A botanical extract may help manage hair loss from chemotherapy by preventing cell death in hair follicles.

The tumor on the man's nose was a rare type called pedunculated follicular hamartoma.

A new mutation in the ST14 gene was found in a patient with ARIH syndrome, showing milder symptoms and no tooth issues.

The pseudo 'fringe sign' can also appear in frontal fibrosing alopecia, not just in traction alopecia, showing that this condition may be more common than thought.

Finasteride significantly reduced tics and obsessive-compulsive symptoms in patients with Tourette syndrome.