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

Vitamin B12 deficiency can cause reversible hair color loss in children.

A rare skin condition with dark, thick, warty patches and some hair loss was found in a newborn boy.

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

Hair can regrow in adult mice's skin after injury, and this process can be boosted by increasing Wnt7a, a protein. This could potentially help treat baldness and change our understanding of hair growth.

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

Older women face various skin issues like dryness and thinning, and treatments are available but can have side effects; proper skin care and legal health decisions are important.

A girl with Netherton syndrome was able to eat wheat without allergies after a special treatment.

A patient with Wilson's disease showed hair-pulling behavior as an initial symptom.

Brandt syndrome, with symptoms like skin rash, hair loss, and diarrhea, improves quickly with zinc supplements.

Adults with Tatton-Brown-Rahman syndrome may have serious heart problems and need lifelong heart monitoring.

The document concludes that individualized treatment and lifestyle changes are important for managing menopause symptoms and health risks.

The term "Porokeratotic Adnexal Ostial Nevus" is suggested as a more appropriate name.

Tight junctions create a barrier in pig hair follicles that controls what can enter the skin.

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 various disorders can cause hair loss in dogs, each requiring different treatments, and some may heal on their own.

Mice without the vitamin D receptor gene lose hair due to disrupted hair follicle cycles.

Fine needle aspiration with rapid on-site evaluation is useful for diagnosing pilomatrixoma.

Androgen lowering medications don't significantly change HCV-related liver cancer risk in men.

Different PCOS types respond uniquely to infertility treatments, with some having lower pregnancy rates and higher risks of complications.

The infant with a urea cycle disorder improved with treatment and a liver transplant.

Conditions affecting sex development show that sexual diversity is a natural part of human variation.

A genetic mutation in the SGK3 gene causes hairlessness in Scottish Deerhounds and may relate to human hair loss.

A 3-year-old girl with skin mast cell buildup and congenital baldness improved with treatment, suggesting a rare link between these conditions.

A 2-year-old boy had no hair and unusual organ placement, and it's unclear if it's genetic or coincidental.

A new mutation in the PLEC gene causes a rare condition with skin blistering, muscle weakness, and hair loss.

Three siblings with a genetic form of rickets showed different symptoms of the disease.

High levels of testosterone and anti-Müllerian hormone before pregnancy are linked to a higher risk of newborns needing intensive care.

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.

Mice with too much Claudin-6 have skin barrier problems and abnormal hair growth.