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Using cheek skin and cartilage grafts for nose reconstruction after skin cancer surgery can maintain shape and function but may require multiple surgeries and hair removal in men.

Two specific SNPs in the TRPS1 gene cause excessive hair growth by altering the protein's structure.

Spiny keratoderma is a rare skin condition with small spines on palms and soles, possibly linked to abnormal hair formation.

Antifungal treatment can improve severe skin infections with cutaneous horns.

The EDAR gene mutation leads to thinner and more deformed hair shafts.

The curly mutation in SELH/Bc mice affects hair and may help study human genetic disorders.

A white-tailed deer fawn in South Dakota was the first cervid found with congenital hypotrichosis, a condition causing sparse or missing hair.

A woman with a rare hormone resistance condition also had missing teeth and hair loss, which might be new symptoms of her genetic disorder.

People with Lichen Planus have thicker carotid artery walls, but it's not solely due to Lichen Planus when other factors are considered.

Tight traditional hairstyles can cause hair loss.

Large-scale reconstructions enhance understanding of vibrissal sensory mapping in the brain.

A deer fawn in South Dakota was the first cervid found with congenital hypotrichosis, a condition causing sparse or missing hair.

Compound follicles in folliculitis decalvans mainly have active hair follicles.

A new mutation in the TRPS1 gene was found in a Ukrainian girl with Trichorhinophalangeal syndrome type I.

The patient's hair was thinner and had fewer lipids due to a genetic mutation.

The new hairline classification and correction methods can improve the appearance of Asian women with wide or M-shaped foreheads.

Older thin hair is not just thinner but also has different shape, structure, and stiffness.

Congenital triangular alopecia is a harmless, non-spreading hair loss condition often seen in young children.

Get head MRI for babies with achondroplasia early, use free immunoglobulin light chains to detect certain neurodevelopmental disorders, and video calls work for speech therapy in patients with facial anomalies.

A man's crushed thumb caused unusual horizontal nail ridges on all fingers of one hand.

The document suggests "anisotrichosis" as a new term for hair thickness variation in common baldness.

Surgical treatment for cubital tunnel syndrome can be effective using clinical tests without electrodiagnostics.

A rare cataract surgery complication was successfully treated with laser capsulotomy.

Hair-shaft abnormalities can indicate neurological disorders, some of which are treatable.

Basonuclin 2 is vital for the development of facial bones, hair follicles, and male germ cells in adult mice, and its absence can lead to dwarfism and abnormal follicles.

Siblings with signs of virilization should be tested for non-classical congenital adrenal hyperplasia, which does not affect adult height but may impact fertility and well-being if untreated.

Variation in the TCHH gene affects wool curliness in sheep.

Older Julia Creek dunnarts often have reproductive and hormonal health issues.