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Some treatments for folliculitis decalvans work well, with tetracyclines and a mix of rifampicin and clindamycin being most effective.

Some families have a genetic condition where they are born with irregular scalp defects.

The L457(3.43)R mutation in the human lutropin receptor causes increased activity and hormone insensitivity, leading to precocious puberty.

Childhood ptosis can vary from a minor cosmetic issue to a serious condition and may signal other health problems.

Indian Hedgehog helps control skin cell growth and protects against aggressive skin cancer.

Reduced androgens linked to kinky hair disorder and hair loss; 5a-reductase inhibitors may help.

A rare skin disorder, Ichthyosis with confetti, has no cure but treatment focuses on managing symptoms with moisturizers.

Pharmacy-sold shampoos tend to have fewer allergens compared to those sold in other stores.

A 13-year-old boy had a rare, stable type of hair loss with little chance of regrowth, but treatment is available for looks.

The study found that Temporal Triangular Alopecia often starts in early childhood, mainly affects the left side of the scalp, and has no effective treatment except surgery.

Skin symptoms can indicate endocrine disorders and have various treatments.

Uncombable hair syndrome causes frizzy hair and can affect the nervous system, eyes, and ears, often co-occurring with other hair, skin, nail, and teeth conditions, and is linked to three specific gene mutations.

Vitiligo is a skin condition causing white spots, more common in women, often starts before age 20, and can affect mental health.

There are many treatments for permanent hair loss disorders, but their effectiveness varies and there's no clear best option.

Mice studies show that Protein Phosphatase 2A is crucial for cell growth, development, and disease prevention.

The skin protects the body and is constantly renewed by stem cells; disruptions can lead to cancer.

The document concludes that understanding and treating hair loss requires recognizing its various types and using appropriate diagnostic tools and treatments.

Assessing newborn scalp hair can reveal important health information.

Adrenal disorders can cause lasting brain and behavior issues in children.

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

The cause of atypical Cushing's syndrome in dogs, possibly linked to sex hormones, is not yet proven.

The document says menstruation is important for women's health, discusses menstrual disorders, and suggests personalized treatment options.

A 2-year-old boy with a rare brain malformation may have Gomez–López-Hernández syndrome.

Skin abnormalities can indicate immunodeficiency due to shared origins with the immune system.

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

Most hair loss in children is caused by a few common conditions and is easy to diagnose, but rare types require careful evaluation.

Certain mutations in the PADI3 gene may increase the risk of developing a type of scarring hair loss common in women of African descent.

Scalp basal cell carcinoma may be more aggressive and harder to treat than other types, requiring special attention and further research.

The Wnt signaling pathway is not a major factor in the development of keratoacanthoma, a type of skin tumor.

The document explains the genetic causes and characteristics of inherited hair disorders.