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A specific genetic change is linked to mental disorders, intellectual disability, and possibly autoimmune disease in a family.

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

A 5-year-old boy was diagnosed with congenital triangular alopecia, a type of hair loss without skin changes, usually starting between ages 2-5, with no specific treatment.

The girl has both monilethrix and Type 1 diabetes, but no link between the two conditions is known.

Carriers of a specific gene mutation have subtle skin changes without visible symptoms.

Dogs exposed to their owners' hormone therapy developed hair loss, but symptoms resolved after stopping the therapy.

Thyroid hormone affects skin health, with too little causing rough, pale skin and too much leading to smooth, thin skin, and may also impact wound healing and skin conditions.

Childhood and adult height, and early immune-related hospitalizations increase testicular cancer risk, while baldness, larger families, and sports reduce it.

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

Loss of Dnmt3a and Dnmt3b increases aggressive skin tumors by affecting PPAR-γ.

A 13-year-old boy with Cushing syndrome has high cortisol levels from a pituitary gland issue and underdeveloped sexual characteristics.

Regulatory T cells help prevent autoimmunity and have potential for treating autoimmune diseases.

Early recognition of skin lesions in Birt-Hogg-Dubé syndrome is crucial for detecting renal tumors early.

Excessive body hair can signal complex health issues.

Levothyroxine treatment fully cured the young man's hypothyroid symptoms.

A boy with a rare form of early puberty caused by a new gene mutation responded well to treatment aimed at reducing testosterone and preserving adult height.

Trichodysplasia spinulosa can occur after a heart transplant due to immunosuppressive drugs.

A woman with X-linked chronic granulomatous disease developed lupus-like skin lesions, improved with treatment, suggesting a unique skin condition in carriers.

A potential link exists between unexplained hormone deficiency, hair loss, and testicular tumors, suggesting thorough screening is needed.

Thymosin beta 4 protects cells from damage by blocking a harmful microRNA and boosting a protective gene.

Prepubertal girls with hypertrichosis have more sensitive androgen receptors, leading to increased body hair growth.

Higher thyroid hormone levels may be linked to certain types of polycystic ovary syndrome.

A child with Sweet syndrome was found to have chronic granulomatous disease and improved with treatment.

Celiac disease can cause thyroid medication malabsorption, and a gluten-free diet can help stabilize thyroid levels.

The boy likely has a fungal infection causing hair loss.

γδ T cells help control tissue scarring and blood vessel growth in response to foreign objects.

Hairy elbows may be linked to short stature, but the exact cause is unclear.

Nearly half of children with primary immunodeficiency disorders showed skin problems, often as the first sign of their condition.

A 19-year-old male with delayed puberty was successfully treated for a condition that prevents normal hormone production.