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

A rare ovarian tumor can cause unusual male-like symptoms, but surgery usually leads to a good outcome.

Congenital Triangular Alopecia is a rare, non-scarring hair loss that can be surgically treated in females for cosmetic reasons.

A woman's mature cystic teratoma caused her virilization by producing testosterone.

Steatocystoma multiplex is a skin condition starting around age 26, linked to hair follicles, and related to eruptive vellus hair cysts.

Somatic BHD mutations are rare in Japanese renal tumors.

Congenital atrichia with papular lesions is often misdiagnosed, and new diagnostic criteria can improve accuracy.

The cyst had unusual keratin spherules and resembled bone marrow.

A 21-year-old male has a benign skin condition called Becker's nevus, which he chose not to treat.

A standardized scoring system is needed to improve model reliability for predicting hair loss in brain tumor patients treated with proton therapy.

The research created a detailed map of skin cells, showing that certain cells in basal cell carcinoma may come from hair follicles and could help the cancer grow.

A child with ectodermal dysplasia-syndactyly syndrome has a new mutation in the NECTIN4 gene.

Targeting NMMHC IIA may help treat blood-brain barrier damage.

Scientists found a new protein, AMY117, common in Alzheimer's patients, which could be important for treatment and diagnosis.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

A woman's pelvic pain and bleeding led to finding and successfully treating a rare benign tumor in her reproductive system.

Trichilemmal carcinoma can spread to the parotid gland and be diagnosed using fine-needle aspiration cytology.

A woman's unique dementia was misdiagnosed, a genetic mutation increases Parkinson's risk with age, and finasteride may help with Tourette syndrome.

A new genetic mutation in the TRPS1 gene causes Trichorhinophalangeal Syndrome, leading to specific hair, dental, and bone issues.

A gene called APCDD1, which controls hair growth, is found to be faulty in a type of hair loss called hereditary hypotrichosis simplex.

The review found that basal cell carcinomas on the scalp are not more aggressive than those in other locations.

SACUMAN, a rare condition causing hair loss without clear signs, is often misdiagnosed and needs scalp biopsies for accurate detection.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

A rare scalp infection in a child developed into a kerion with additional skin symptoms.

The research found that a specific gene mutation causes fewer hair follicles and disrupted hair growth cycles, leading to thin and short hair in people with Hypotrichosis with Juvenile Macular Dystrophy.

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

BMP4-related anomalies can cause a wide range of eye, brain, and hand/foot problems, and new cases show this variability.

A family showed a new condition with inherited hair loss and skin changes, possibly due to one genetic disorder.

A Turkish family with sparse hair and eyebrow loss has a mutation in the U2HR gene linked to Marie Unna hereditary hypotrichosis.

Alopecia areata patients show unique protein activity patterns, suggesting imbalanced signaling pathways.