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Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

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

Folliculotropic mycosis fungoides can occur in children and is diagnosed with specific tests, but often stays in early stages with treatment.

Certain mouse strains develop a skin condition similar to a human hair loss disease due to genetic defects.

A rare skin condition caused scarring hair loss on the scalp.

Cronkhite-Canada syndrome can be diagnosed without gastrointestinal polyps if there is severe mucosal atrophy and edema.

The boy's genetic diagnosis of ectodermal dysplasia helped improve management and counseling for him and his sister.

Rapp-Hodgkin syndrome, AEC, and EEC are different expressions of the same genetic disorder caused by TP63 gene mutations.

The GH-IGF-I axis is likely involved in the hormonal imbalances seen in non-obese women with functional hyperandrogenism.

Combination therapy with steroids and pimecrolimus improved or stabilized hair loss in most patients with Frontal Fibrosing Alopecia, who also had a high rate of hypothyroidism.

Skin problems like acne and excess hair in PCOS are common and linked to being overweight.

Genetic testing for hairless gene mutations is crucial to correctly diagnose and treat atrichia with papular lesions.

A unique type of hair loss mimics another condition but has minimal inflammation and specific immune cells present.

Genetic testing is crucial for diagnosing congenital atrichia, a rare condition causing irreversible hair loss.

Myotonic dystrophy may be classified as a segmental progeroid disorder.

Recognizing unusual symptoms in Crohn's disease is crucial for proper treatment.

Genetic factors influence hair traits like shape, color, and greying in Latin Americans.

Fibrosing alopecia can be stabilized or improved with anti-inflammatory treatments and hair growth agents.

Researchers found a new mutation causing total hair loss from birth.

A genetic marker linked to a type of hair loss was found in most patients studied.

Tailored treatments for aging brows and foreheads improve results.

Trichofolliculoma was found in a person with amniotic band syndrome for the first time.

Frontal Fibrosing Alopecia is a poorly understood condition that is hard to treat and causes distressing hair loss.

A multidisciplinary approach is crucial for treating complex cases of Rapunzel syndrome in children.

Temporal triangular alopecia is a non-scarring hair loss seen in some Asian children.

A 5-year-old girl with McCune-Albright syndrome grew abnormal hair due to the drug tamoxifen.

Advanced male pattern baldness affects the back of the scalp, reducing hair follicles.

Possible endocrine disorders caused woman's hair loss and obesity in painting.

Severe acne in a young girl may indicate underlying hormonal issues.