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The document concludes that PCOS is a complex disorder caused by both genetic and environmental factors, affecting women's health in various ways, and requires personalized treatment.

Some women with excess hair growth have a hormone condition that can't be diagnosed by blood or urine tests alone.

Higher androgen levels during puberty are linked to shorter adult height in boys with Silver-Russell syndrome.

VEGF helps squamous cell carcinoma grow in ways beyond just blood vessel formation.

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

Acne is a common skin condition linked to diet, hormones, and genetics, and early treatment can prevent scarring.

Normal-range ALT levels can indicate metabolic and hormonal imbalances in young women.

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

A 3-year-old boy was diagnosed with a rare, non-scarring hair loss condition called temporal triangular alopecia.

The review concludes that accurate diagnosis of different types of hair loss requires proper biopsy techniques and understanding the hair growth cycle and underlying causes.

Hirsutism is mainly caused by high androgen levels or sensitivity, with PCOS being the most common cause.

A rare ITGB6 gene variant causes intellectual disability, hair loss, and dental issues.

Finasteride use during early pregnancy may cause limb deformities in babies.

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

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

A 23-year-old Syrian woman has two rare hair disorders, and avoiding hair treatments plus using vitamins and minoxidil may help.

The document concludes that permanent hair loss conditions are complex, require early specific treatments, and "secondary permanent alopecias" might be a more accurate term than "secondary cicatricial alopecia."

Loss of Msx2 function causes eye development issues similar to Peters anomaly.

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

Long-term oral and topical treatments improved skin condition in a goldendoodle with a genetic disorder.

Gene mutations can cause problems in male genital development.

Defects in certain proteins cause major heart abnormalities during early development.

Trichoscopy is a useful non-invasive method for diagnosing different hair loss conditions.

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

Simvastatin may help manage symptoms in women with non-classic congenital adrenal hyperplasia by lowering cholesterol and certain hormone levels.

A specific genetic change in the KRT71 gene causes a hair loss condition in Hereford cattle.

The conclusion is that a thorough approach is needed to diagnose and manage hyperandrogenism in teenage girls, recognizing its major psychological and health effects.

Some parents have a mild form of congenital adrenal hyperplasia without symptoms, and they usually don't need treatment.

AMH levels can't reliably tell the difference between LOCAH and all types of PCOS in women with excessive hair growth.

Trichoscopy is a quick and easy way to diagnose most genetic hair problems without invasive methods.