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The analysis found that alopecia areata, a hair loss condition, is not very common in Australia, affecting about 0.13% of people, with new cases most often seen in males aged 19 to 34 years.

The case suggests that dissecting cellulitis of the scalp can occur in a White child and should be considered when diagnosing pediatric scarring alopecia.

Low iron levels are linked to hair loss in women.

The baby’s hair loss was due to a rare genetic condition, not treatable by usual methods.

The document concludes that an experimental drug may help wound healing in Epidermolysis Bullosa, links Hydroa vacciniforme to EBV, discusses diagnosing hair loss disorders, finds many children with eczema have allergies, reviews the safety of a skin medication in children, notes side effects of a Duchenne's treatment, and identifies a marker for pediatric mastocytosis.

The document concludes that a thorough history, physical exam, and specific tests are crucial for diagnosing and managing hair loss effectively.

Using 5% topical minoxidil improved and normalized the hair growth in a girl with short anagen hair naevus.

Different hair fiber development might explain why hair loss severity varies in patients with a specific genetic mutation, and treatments that thicken hair could help.

A new hair loss treatment was created using minoxidil and tretinoin in stable niosomes, which effectively released the drugs over time.

Untreated Congenital Adrenal Hyperplasia can cause severe hair loss due to high androgen levels.

A genetic marker linked to a type of hair loss was found in most patients studied.

A man with a birthmark on his scalp developed hair loss that improved with treatment, but the link between the birthmark and hair loss was unclear.

Black dots under trichoscopy can appear in different hair and scalp conditions, not just in alopecia areata.

The document concludes that diagnosing and treating Congenital Adrenal Hyperplasia is complex and requires a team approach due to its effects on the skin and other symptoms.

AGA in children needs careful diagnosis due to low androgen levels and possible other causes.

Two Australian Poll Hereford calves had severe anaemia, abnormal red blood cells, and skin issues.

The painting of an 18th-century Sicilian baroness shows she had hair loss, possibly due to ovarian issues, insulin resistance, or a specific type of tumor.

Minoxidil is effective in treating various types of hair loss and can improve quality of life, with combination therapies showing increased effectiveness.

Different genes are linked to various types of hair loss.

New genotype linked to non-classical congenital adrenal hyperplasia found in Italian siblings.

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

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

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

New ABCA12 gene mutations were linked to a skin condition with scaling and hair loss, and a treatment helped with hair loss in a related case.

The top research priorities for congenital ichthyosis include long-term side effects of oral retinoids, best topical treatments, and treatments for itch and hair loss.

A woman with Kallman's syndrome also developed alopecia universalis, a condition not previously linked to Kallman's.

A Brazilian male with IFAP syndrome has a unique genetic variant causing his condition.

The twins' condition is unique and doesn't match any known syndromes.

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