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Rapamycin and anti-EGFR antibody reduce LAM/TSC cell migration and blood vessel growth in the uterus.

The girl's skin condition is benign but challenging to treat due to its size and location.

Mutations in the LIPH gene cause woolly hair in a child.

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

A clinically suspected melanoma appeared benign under the microscope but was confirmed by specific tests and a rare mutation.

Uterine leiomyomas don't significantly change gene expression in the scalp of people with Central Centrifugal Cicatricial Alopecia.

HLD10 can include increased body hair and Mongolian spots.

A woman's severe hirsutism was caused by Leydig cell tumors in her ovaries, which improved after surgery.

Certain gene mutations in Japanese people are linked to different types of hair loss, with some causing mild hair thinning and others leading to complete baldness.

A rare skin condition in a boy is likely due to a specific genetic mutation pattern.

Congenital adrenal hyperplasia may be linked to adrenal myelolipoma.

A new mutation in the KRT86 gene causes monilethrix in a Han family.

A mutation in the KRT86 gene causes hair fragility in a Turkish family.

Combining medication and minimally invasive techniques can effectively manage Marine-Lenhart syndrome.

Matrical tumors share a common growth mechanism involving the Wnt pathway and consistent PHLDA1 expression.

A mare had severe symptoms and died from a large lymphoma.

A new mutation caused a rare hair disorder in a Polish girl, not inherited from her family.

Polyomavirus A2 infection in newborn mice caused hair follicle tumors.

Bilateral ovarian hyperthecosis is a rare but treatable cause of increased facial hair in postmenopausal women.

Monilethrix causes brittle hair and hair loss, and it runs in families.

A man had a non-cancerous, fast-growing skin lump on his arm that was removed with surgery.

Coinheritance of BRCA2 and CYLD genes may lead to new treatment options for certain cancers.

Myotonic dystrophy should be considered in patients with hair thinning, and genetic counseling is important.

A postmenopausal woman's hirsutism and high testosterone levels improved after surgery for an ovarian tumor not seen on ultrasound.

Multiple pilomatrixoma may indicate Turner syndrome.

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

A 5-year-old girl with a rare genetic disorder, lipoid proteinosis, showed reduced new lesions but persistent scars after avoiding skin trauma.

Surgery removed an ovarian tumor, improving her symptoms and normalizing testosterone levels.

A rare ovarian tumor was found in a young woman with a genetic fat disorder.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.