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Dupilumab improved hair and skin in a woman with Netherton syndrome.

Hair changes and a high occipital hairline may help diagnose Trichorhinophalangeal Syndrome.

Eating disorders can cause various hair problems, and while hair loss in these disorders is linked to metabolic syndrome, treatment focuses on specific medications and lifestyle changes for the syndrome.

Plica neuropathica is a tangled hair condition that may be caused by hair damage or psychiatric issues and is treated by cutting the hair and addressing mental health.

Lupus can affect the scalp and nails, often causing hair loss and nail damage, and needs early aggressive treatment to prevent permanent damage.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

Substance P may play a role in the inflammation seen in keratosis follicularis spinulosa decalvans.

Hair loss condition FFA was seen before the appearance of skin depigmentation vitiligo in a patient.

A woman's skin symptoms led to a diagnosis of systemic AL amyloidosis, but she died from sepsis shortly after.

Hair casts can be treated with physical removal and special shampoos.

Isolated patchy heterochromia with pili annulati can occur without other health issues.

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

The patient's symptoms improved with treatment but recurred when the steroid dose was reduced, requiring ongoing therapy.

Consider necrolytic acral erythema in similar cases and treat with oral zinc sulfate.

A patient with hair loss condition grew excessive hair in areas covered by a cast.

Perifollicular erythema can indicate active frontal fibrosing alopecia.

The supplement improved hair, skin, and nails appearance and had long-term benefits.

Two newborns with rare skin infections were successfully treated with antifungal cream.

A new type of pachyonychia congenita linked to a specific keratin gene mutation was found in two Pakistani families.

A woman with a unique syndrome similar to TRPS has a genetic change near the TRPS1 gene, affecting its regulation.

Mice with the 'lanceolate hair' mutation have abnormal hair and skin similar to human Netherton's syndrome.

A 16-year-old boy's arm hair grew more after wearing a splint, but it returned to normal in 8 months.

A patient with Cronkhite-Canada syndrome improved with nutritional support and steroids, but early diagnosis is key due to high mortality.

Early diagnosis of frontal fibrosing alopecia is crucial to prevent permanent hair loss.

TAF can be identified by excessive skin thickening and clogged hair follicles, helping distinguish it from similar skin conditions.

A young boy's uncombable hair is due to a rare genetic condition that usually improves over time.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

The patient's hair had unique damage and a lower sulfur-to-nitrogen ratio compared to relatives, but not compared to healthy controls.

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