Search

everythinglearnresearchcommunity

for

Search:↓

Temporal triangular alopecia causes permanent hair loss and can be managed with treatments like minoxidil or hair transplantation.

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

A rare non-cancerous tumor that grows like hair was found in an unusual spot, the vulva.

An 8-year-old girl has a rare, irreversible hair loss condition caused by a genetic mutation.

A rare genetic mutation caused severe symptoms in a 6-year-old girl with mandibuloacral dysplasia type A.

A new gene mutation causes vitamin D-resistant rickets and hair loss in two siblings.

Hair transplants can be used for rare types of scarring hair loss.

A rare skin condition appeared on a 19-year-old woman's scalp.

CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

A 17-year-old girl with Kartagener's syndrome also has unusual skin, hair, and nail issues.

Mutations in the hairless gene cause hair loss and skin cysts in rhesus macaques.

A child with a rare type of rickets showed some improvement with high doses of vitamin D, but such conditions often respond poorly to treatment.

A girl with a rare genetic disorder had a unique bone condition, highlighting the need for careful diagnosis and suggesting the disorder might be more common than thought.

Trichobezoars can cause serious health issues like biliary obstruction, and treatment includes surgery and therapy to prevent recurrence.

A rare genetic mutation causes resistance to vitamin D, leading to severe rickets and requires high doses of calcium and vitamin D for management.

A 4-year-old girl had a rare hair disorder affecting only part of her scalp.

A 5-year-old girl with a rare skin disorder was effectively treated with skin creams instead of oral medication.

A patient with Rhupus was diagnosed with Rowell syndrome and treated with various medications.

A rare EGFR mutation in newborns leads to severe health issues and early death.

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

Accurate diagnosis and management of rare genian fistulas require combined clinical, radiologic, and histopathologic evaluations.

An 8-year-old girl with Rapunzel syndrome had a hairball removed from her stomach and intestines and recovered well after surgery.

RORA plays a key role in controlling seasonal hair molting by affecting hair follicle cell activity.

A 15-year-old girl with rare reproductive disorders received hormone therapy to develop secondary sexual traits, but infertility persisted.

Dermoscopy quickly and accurately diagnosed a rare hair disorder in a 12-year-old girl.

Pincer nails are rare in lupus patients and may be managed conservatively.

A 29-year-old woman with symptoms of both lupus and rheumatoid arthritis improved with specific medications.

Recognizing scalp symptoms in PRP is crucial for proper diagnosis and treatment.

A 2-year-old boy was diagnosed with a rare genetic condition causing fragile hair, intellectual issues, and short stature.

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