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A new genetic mutation causes severe Leydig cell hypoplasia, affecting sexual development.

GAPO syndrome causes growth issues, hair loss, missing teeth, and vision problems.

A 5-year-old boy was diagnosed with congenital triangular alopecia, a type of hair loss without skin changes, usually starting between ages 2-5, with no specific treatment.

A postmenopausal woman's hair loss and excess hair growth improved after surgery for ovarian hyperthecosis.

Hair-related body dysmorphic disorder is common in hair loss patients and needs early recognition for proper treatment.

The position of the parietal whorl can predict safe donor areas for hair transplants in Korean men with male pattern baldness.

Polycystic Ovary Syndrome should be seen mainly as a condition of excess male hormones, with a focus on this in its definition.

HBCs in the olfactory epithelium can self-renew or differentiate into other cell types, with specific patterns during regeneration.

Early diagnosis and surgery can improve symptoms of ovarian hyperthecosis in postmenopausal women.

Common variants in the Trichohyalin gene are linked to straight hair in Europeans.

Women with hyperandrogenism, especially those with PCOS, are more likely to have psychiatric disorders.

The gene for Clouston syndrome in a large Indian family is located in the 13q11-q12.1 region.

The mutated hairless gene causes hair loss by acting as a new type of corepressor affecting thyroid hormone receptors.

Keratin gene clusters in humans and marsupials are similarly organized.

The TT/DHT ratio may help identify PCOS patients with severe metabolic issues.

New mutations in hair keratin genes cause the rare hair disorder monilethrix.

About 21.3% of young, healthy Chinese men experience hair loss. Hairlines are mostly linear or have a central protrusion. Hair is densest on the top and back of the head, and hair follicles usually have 1 or 2 hairs. This information can help in designing hair restoration procedures.

A 4-year-old girl had a rare hair disorder affecting only part of her scalp.

Some people with schwannomatosis have a new type of mutation in the LZTR1 gene.

K6hf is a unique protein found only in a specific layer of hair follicles.

The type of PCOS a woman has doesn't strongly predict her skin or metabolic symptoms; obesity is a more important factor.

The Oat mouse model shows mild retinal degeneration, useful for testing treatments.

4-O-Methylhonokiol helps protect skin cells from growth-stopping effects of a protein by regulating growth-related pathways.

Custom-designed implants effectively repaired skull damage in most soldiers injured in combat.

The modified Crawford technique resulted in less lagophthalmos and better cosmetic outcomes for patients with lateral droop.

Low TRPS1 expression in skin and hair cells is linked to hair problems in Trichorhinophalangeal syndrome.

The authors agree they didn't follow the original criteria strictly but found the Ottawa rule effective in all tested patients and suggest it might have wider use.

A unique case of skin cancer showed unusual calcification, possibly linked to calcium-binding proteins.

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

The model improves understanding of androgen interactions by focusing on signal intensity and system capacity.