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The study found genetic differences related to hair development that may explain hair loss in a patient with Trichorhinophalangeal syndrome type I.

Orange spots in scalp trichoscopy can help diagnose scalp sarcoidosis.

Netherton syndrome in a boy caused skin and hair issues, and treatment didn't work.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

Doctors often miss Hair Tourniquet Syndrome, which can lead to serious damage if not treated quickly.

Trichoscopy is a useful, painless tool for diagnosing and monitoring children's hair and scalp issues.

Satoyoshi syndrome symptoms can improve with corticosteroids and surgery.

A 6-year-old boy developed excessive hair growth after taking diazoxide for low blood sugar.

Clouston syndrome can lead to skin cancer, so monitoring is crucial.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

Patchy hair loss from post-herpetic neuralgia can mimic trichotillomania but requires different treatment.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

Hair loss in Clouston's syndrome improved with minoxidil and tretinoin treatment.

A 9-year-old girl has a rare hair disorder causing beaded, sparse hair.

The woman has a rare skin condition called follicular Dowling-Degos disease, which has limited treatment options.

A boy with monilethrix has brittle hair that breaks easily due to a genetic condition, which might improve by puberty.

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

Generalized trichoepitheliomas with alopecia may indicate myasthenia gravis.

Trichoscopy is a tool for detailed examination of hair and scalp diseases.

Identical twins with a rare KRT 86 gene mutation both have the hair disorder monilethrix.

A hair strand caused a rare case of limb strangulation in a teenage girl with autism, and the condition is not always linked to child abuse.

Hair examination is crucial for diagnosing Netherton syndrome in patients with certain skin symptoms.

A new genetic variant causes trichothiodystrophy in two brothers, but their mother may carry it without showing symptoms.

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

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

The 'Swiss cheese' pattern in scalp biopsies can indicate trichotillomania, not just alopecia areata.

A new classification for trichothiodystrophy helps identify genetic causes and potential treatments.

A 10-month-old boy with a rare combination of genetic conditions has severe immune deficiency and treatment challenges.

CDH3-related disease causes worsening eye and hair issues.

The girl has an inflammatory type of scarring hair loss.