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Environmental factors can cause mutations in skin proteins, leading to skin disorders.

Recognizing congenital triangular alopecia is crucial to avoid unnecessary treatments.

The severity of symptoms in nonclassical congenital adrenal hyperplasia is not determined by CYP21A2 gene variations.

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

Acne is significantly influenced by genetics, and understanding its genetic basis could lead to better, targeted treatments.

Congenital triangular alopecia is a harmless, non-spreading hair loss condition often seen in young children.

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

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.

Some congenital hair disorders improve with age and can be managed with treatments like minoxidil, retinoids, supplements, and gentle hair care, but there's no cure.

Alopecia areata, a common autoimmune hair loss condition, often runs in families.

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

The conclusion is that PCOS is a common cause of hirsutism in young obese women, and early treatment is important to reduce the risk of metabolic syndrome.

Oral retinoids can cause side effects ranging from mild to severe, including birth defects, and require careful monitoring and contraception.

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

Finasteride affects male rat genitalia development, causing abnormalities during specific pregnancy days.

The document concludes that understanding hair structure is key to diagnosing hair abnormalities and recommends gentle hair care for management.

Coats' Plus is a genetic disorder with eye abnormalities, brain calcification, poor growth, bone and skin issues, and movement disorders.

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

New genetic mutations linked to rare skin disorders were found in three newborns.

The document concludes that a systematic approach is crucial to identify causes of androgen excess in women beyond the most common cause, Polycystic ovary syndrome (PCOS).

The document explains how to identify different hair problems using a microscope.

Acne is linked to inflammation and insulin resistance, and is associated with various syndromes that require different treatments.

The chapter explains that there are many genetic skin disorders affecting skin cell formation, including both common and rare types.

Hirsutism in teens is often due to polycystic ovarian syndrome and needs careful assessment and support.

Some ovarian tumors can cause masculinization, and it's important to check for various causes when this symptom is present.

Diabetes can lead to blindness and skin problems, and managing blood sugar and blood pressure is crucial to prevent these complications.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

The conclusion is that accurately identifying the cause of high androgen levels in women with PCOS is crucial and requires specific tests.

Congenital Adrenal Hyperplasia is a genetic disorder with two forms, causing symptoms like early puberty and severe acne, but can be identified through screening and treated with glucocorticoids.

Early diagnosis and treatment of hereditary vitamin D-resistant rickets (HVDRR) are crucial to prevent growth issues and other health problems.