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Accurate diagnosis of EFFC is crucial for effective counseling and cosmetic care.

cGVHD often severely affects the skin, causing rapid aging and other issues.

A patient with Rothmund-Thomson syndrome showed skin changes, hair loss, and dental defects but no cataracts or skeletal issues.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

The patient's hair had unique damage and a lower sulfur-to-nitrogen ratio compared to relatives, but not compared to healthy controls.

Frontal Fibrosing Alopecia may be linked to autoimmune diseases like Sjögren's syndrome.

A 44-year-old woman with Down's syndrome was diagnosed with both rheumatoid and gouty arthritis and treated with multiple medications.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

Many women with postadolescent acne also have hormonal imbalances and are at higher risk for metabolic issues.

A golden lion tamarin had Cushing's disease due to a pituitary tumor, leading to its euthanasia.

The girl has an inflammatory type of scarring hair loss.

The girl's unexpected pubic hair growth led to a diagnosis different from complete androgen insensitivity syndrome.

Excessive body hair can signal complex health issues.

A new mutation in the MBTPS2 gene causes a mild form of IFAP syndrome.

A 20-year-old woman with a rare form of Turner syndrome showed improvement with hormonal therapy and needs comprehensive care.

Asian patients with Frontal Fibrosing Alopecia often lose eyebrow hair and respond well to combined antiandrogen or antimalarial and topical treatments.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

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.

An 11-year-old obese girl was diagnosed with lipedematous scalp, a condition with swollen scalp tissue usually found in adult women.

A man with Woolly Hair Syndrome had very curly, fragile hair, and doctors used a special scalp examination to diagnose him without invasive tests.

A girl with a rare skin condition improved after one month of treatment with acitretin.

Men with a certain type of hair loss (vertex type AGA) may have higher levels of bad fats (triglycerides) and lower levels of good cholesterol (HDL), suggesting they could be at risk for high fat levels in the blood (hyperlipidemia).

Hair varies in size and features depending on body region.

Most women with hyperandrogenism first show acne, and skin conditions like hirsutism and acanthosis nigricans are good indicators of the condition.

The GH-IGF-I axis is likely involved in the hormonal imbalances seen in non-obese women with functional hyperandrogenism.

A Japanese patient with IFAP syndrome had a severe MBTPS2 gene mutation but showed milder symptoms than previously observed cases.

A 15-year-old boy had a rare skin growth on his buttock.

A woman had both Graham Little-Piccardi-Lassueur syndrome, causing hair loss, and complete androgen insensitivity syndrome, making her genetically male but physically female. This suggests androgens don't affect the hair loss condition.

Hair density and thickness decrease in all scalp areas for East Asians with AGA.

A mother and daughter had severe skin, hair, and eye issues linked to IFAP.