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The rise in tinea capitis cases in Stockholm is linked to increased African immigration.

Accurate diagnosis and effective oral treatment are key to managing tinea capitis and preventing its spread.

Biotin supplements improved skin and hair problems in a girl with biotinidase deficiency.

Some children in Malaysia with symptoms have either profound or partial biotinidase deficiency, and early testing and treatment are important.

Early adrenal gland maturation in young children can be normal, but other serious conditions should be ruled out first.

Molecular diagnostics help identify genetic defects causing endocrine diseases, improving diagnosis and treatment options.

New treatments and management strategies for skin conditions like melanoma and Spitz naevi were discussed at the dermatologists' meeting.

An infant with seizures and hair loss was diagnosed with biotinidase deficiency and treated successfully with biotin.

Certain gene variations in AKT2 are more common in women with PCOS and are linked to higher levels of specific hormones and symptoms.

The document concludes that Syndromes of Severe Insulin Resistance are rare disorders with limited treatment options.

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People with Birt-Hogg-Dubé syndrome often have lung problems and delayed diagnosis, and better recognition of CT scan signs could improve diagnosis and management.

Treating a boy's scalp infection was challenging because two different colors of the same fungus appeared.

New LPA receptors (LPA4, LPA5, LPA6) have diverse roles in the body.

A new gene variant in the DSP gene is linked to a unique type of hair loss.

Preventing cancer involves lifestyle changes, vaccinations, early screening, and understanding cancer's molecular basis.

The update highlights that non-classic congenital adrenal hyperplasia is common in women with excess male hormones, requires specific hormone tests for diagnosis, and has various treatment options depending on age and symptoms.

Genetic variation in the androgen receptor gene mainly causes early-onset hair loss, with maternal inheritance playing a key role.

Dermatoscopy and videodermatoscopy are useful for diagnosing and monitoring various skin, hair, and nail conditions.

The paper concludes that drug labels should be clear for all, especially for those with low literacy, and suggests aiming for high comprehension test passing rates with diverse test populations.

Biotin and biotinidase are essential to prevent health issues, and deficiencies require lifelong supplementation.

Hairless gene not strongly linked to baldness.

Children with alopecia areata should only have thyroid screening if they have Down syndrome, a history of atopy, family history of thyroid disease, or signs of thyroid problems.

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

Older age, higher BMI, and family history of diabetes increase the risk of gestational diabetes in pregnant women.

Children with alopecia areata should only get thyroid screening if they have Down syndrome, a family history of thyroid disease, atopy, or signs of thyroid problems.

Phyllanthus urinaria extract may help treat hair loss by blocking a hair-related enzyme.

A new genetic area linked to a rare hair loss condition was found on chromosome 13 in a Chinese family.

Teens with PCOS have a higher risk of type 2 diabetes and need regular glucose checks.

Men with a family history of hair loss on their mother's side are more likely to have female pattern hair loss.