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Melanocytes are important for normal body functions and have potential uses in regenerative medicine and disease treatment.

Becker's Nevus Syndrome is a rare condition with a skin patch and possible bone and muscle abnormalities, treated mainly for appearance.

A Nigerian baby with neonatal lupus got better with treatment by 6 months.

The report concludes that atypical Brauer nevus is more common in males, present at birth, and often misdiagnosed due to its unusual scalp locations.

Biotin supplements may improve hair and nail growth in people with certain deficiencies or conditions, but there's not enough evidence to recommend it for healthy individuals.

Botulinum toxin shows promise for various skin conditions but requires more research for confirmation and standardized use.

The skin's ability to produce hormones is linked to various skin conditions, and better understanding this process could lead to new treatments.

The sebaceous gland has more roles than just producing sebum and contributing to acne, and new research could lead to better skin disease treatments.

The document concludes that patient outcomes for Congenital Adrenal Hyperplasia are often not ideal because of poor management and a need for better diagnosis and treatment methods.

Twisted hair is rare in severe anorexia nervosa, found in only 2 out of 30 patients.

Early hair loss in men and women may indicate a higher risk of heart disease and metabolic problems.

The document concludes that diagnosing female hair loss requires careful examination, with treatments varying by condition and psychological support often necessary.

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

Hair-thread Tourniquet Syndrome, where hair or thread tightly wraps around a body part, is not rare and requires early detection to prevent serious damage.

Rabbits lacking the Hoxc13 gene show similar hair and skin issues to humans with ECTD-9, making them good for research on this condition.

CAH is a genetic disorder affecting cortisol production and causing hormonal imbalances, with treatment and diagnosis varying by form and symptoms.

Hair transplantation using micrografts and minigrafts is effective and safe for facial and scalp reconstruction with natural-looking results.

Androgenic alopecia causes hair follicle degradation and skin restructuring, but some hair elements remain.

Blond hair in Solomon Islanders is due to a unique genetic variant, not European ancestry.

Hair transplants can cause hair loss if done while lichen planopilaris is active; wait until it's inactive for two years and check with a scalp biopsy first.

Nonclassic congenital adrenal hyperplasia is a common genetic disorder that can cause a range of symptoms and requires personalized treatment.

Mutations in the SRD5A3 gene cause a new type of glycosylation disorder by blocking the production of a molecule necessary for protein glycosylation.

The document concludes that early diagnosis and treatment of Congenital Adrenal Hyperplasia are crucial for preventing serious health issues and improving patient outcomes.

Inherited ichthyoses cause widespread skin scaling and thickening due to gene mutations.

The document concludes that diagnosing and treating Congenital Adrenal Hyperplasia is complex and requires a team approach due to its effects on the skin and other symptoms.

A new gene mutation linked to a skin condition was found in a Spanish family.

Antiandrogen therapies are beneficial for treating skin and hair conditions related to androgen levels.

New genes linked to ichthyosis were found, but there's still no cure; treatment options are improving.

Acitretin helped improve hand mobility and skin condition in a patient.

Hormonal therapies are safe and effective for treating acne in female adolescents, with specific treatments for those with endocrine disorders.