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Chemicals and body size might change when puberty starts and progresses, but more research is needed to confirm this.

Some growth factors, while important for normal body functions, can cause diseases when not regulated properly.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

Androgen receptors are key for development and health, affecting conditions like prostate cancer and male pattern baldness.

The document concludes that proper diagnosis and a multidisciplinary approach are crucial for managing Congenital Adrenal Hyperplasia effectively.

The vitamin D receptor is crucial for bone health and affects various body systems, with mutations potentially leading to disease.

Protoporphyrin IX is useful in cancer treatment but can cause health problems if not properly regulated.

The document concludes that Nonclassic Congenital Adrenal Hyperplasia requires personalized treatment plans to manage symptoms and fertility, with glucocorticoids being a common therapy.

Skin reactions to antidepressants are common but usually not serious and can be treated.

A TP63 gene mutation causes significant hair loss and mild skin, nail, and tooth abnormalities.

Special immune cells called Regulatory T cells help control skin inflammation and repair in various skin diseases.

Growth hormone levels affect hair growth and loss, with too much causing excess hair and too little leading to hair loss.

A rare genetic mutation found in an Indian family can be detected through prenatal screening.

Six genetic conditions are often linked to complete scalp hair loss in children.

A specific gene variant is linked to heart disease, increased heart muscle, curly hair, and thick skin on palms and soles.

Targeted anticancer therapies can cause severe side effects similar to traditional chemotherapy, but with different types.

The ITGB6 gene is important for tissue repair and hair growth, and mutations can lead to enamel defects and other health issues.

Dutasteride, usually used for prostate issues and hair loss, could potentially treat Amyotrophic Lateral Sclerosis (ALS) due to its neuroprotective, antioxidant, and anti-inflammatory properties, but more testing is needed.

Curcuma aeruginosa Roxb. may help treat hair loss by affecting specific biological pathways.

Hair follicles are normally protected from the immune system, but when this protection fails, it can cause hair loss in alopecia areata.

The UD-PrOZA program successfully diagnosed 18% of adult patients with rare diseases, often using genetic testing.

Mutations in TBX3 cause horses to have more even hair color instead of Dun camouflage.

Fibrodysplasia ossificans progressiva is a rare genetic disorder that causes extra bone growth and symptoms of premature aging.

A mouse gene mutation increases the risk of skin cancer.

The TRPV3 ion channel is important for skin and hair health and could be a target for treating skin conditions.

The study found two new mutations in a Chinese patient with severe biotinidase deficiency.

A boy's skin fragility and sparse hair were caused by a genetic mutation affecting skin cell adhesion.

Studying premature aging syndromes helps understand human aging and suggests potential treatments.

High mTORC1 activity slows hair growth and causes it to lose color.

Different STUB1 gene mutations cause varied symptoms in autosomal recessive ataxias.