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Androgens like testosterone are important hormones for both men and women, made differently in each sex and affecting the body by regulating genes and quick interactions with cell components.

Syphilis has a wide range of symptoms that can look like other diseases, and if not treated, it can progress to a more serious stage, especially in HIV-positive patients.

Nonclassic congenital adrenal hyperplasia is a genetic disorder causing hormone imbalances, affecting fertility and requiring personalized treatment.

With careful management, people with congenital adrenal hyperplasia can have successful pregnancies and become parents.

The document concludes that accurate diagnosis of hair loss in children is crucial due to limited treatment options and the condition's psychological impact.

Trichoscopy is reliable for diagnosing Temporal Triangular Alopecia and can prevent unnecessary biopsies and wrong treatments.

Using microneedles before applying eflornithine cream can make it more effective at stopping hair growth.

A mother and son both had ulcerative colitis and alopecia, suggesting a genetic link in autoimmune disorders and successful treatment with cyclosporine.

Minoxidil solution can cause skin irritation and allergies in some users.

A woman developed male traits from accidental contact with her husband's testosterone gel.

EGFR inhibitors can cause various skin issues during cancer treatment, and managing these is important for patient care.

Using buccal mucosa for hypospadias repair in children is effective and reduces complications.

Propranolol is effective and safe for treating infantile hemangioma, but more research is needed for dosing and monitoring guidelines.

Trichotillomania, a disorder where people compulsively pull out their own hair, often starts around age 12, is more common in adult females, and can be treated with behavior therapy and medication.

Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

A rare fungal infection on a child's scalp was successfully treated with antifungal medication.

MC-DNA vector-based gene therapy can temporarily treat CBS deficiency in mice.

Cantú syndrome may be linked to pituitary adenomas.

A woman with HIV had a severe skin condition that improved with antiretroviral therapy.

PCOS is a long-term condition that needs more research for better understanding and treatment.

A person with a specific gene mutation had extra teeth, unique jaw and hair features not seen before in this condition.

Effective symptom management in IBD improves quality of life and prevents complications.

Topical tofacitinib may effectively and safely regrow facial hair in some people with alopecia areata.

Hair tourniquet syndrome in infants can be treated successfully with immediate hair removal.

Certain gene variations might be linked to severe acne in women but not in men.

To prevent and treat Hair-thread tourniquet syndrome in infants, keep a close eye on their limbs, manage maternal hair loss, and educate parents and healthcare providers.

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.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

The document concludes that early diagnosis and a comprehensive treatment plan are crucial for managing hair loss in children, with a focus on both medical and psychological support.