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CARASIL, a rare genetic disorder, was confirmed in an Arabic woman, highlighting its rarity and need for stroke prevention.

Cronkhite-Canada syndrome can be diagnosed without gastrointestinal polyps if there is severe mucosal atrophy and edema.

Psoralea corylifolia (Bakuchi) is effective for treating various health issues, especially skin disorders.

White lupin uses specific genes to grow root hairs and access phosphorus when it's scarce.

A man with hypoparathyroidism had other health issues that led to a diagnosis of a rare autoimmune disorder, APS-1.

The scalp has a natural speckled pattern of increased pigment around hair follicles, possibly linked to local hormone production.

Alopecia areata can look like frontal fibrosing alopecia, making diagnosis hard.

Some people with lichen planus pigmentosus might later develop frontal fibrosing alopecia.

A new pair of mouse keratins, 65 kD and 48 kD, are found in specific skin areas and are linked to a unique skin differentiation type.

Alopecia in gray bats is most common and severe during lactation, likely due to stress and nutrition.

A rabbit gene important for hair development was identified and detailed.

Generalized trichoepitheliomas with alopecia may indicate myasthenia gravis.

A rare skin condition called linear lichen planopilaris caused itchy red bumps and hair loss on a man's face.

A multidisciplinary approach is crucial for treating complex cases of Rapunzel syndrome in children.

Topical minoxidil may help treat a rare genetic hair condition with no fully effective treatments yet.

Cathepsin L deficiency causes hair and skin issues in mice.

Thorough scalp exams are crucial for diagnosing hair loss conditions in people with skin of color.

Mice without the Sept4/ARTS gene heal wounds better due to more stem cells that don't die easily.

GABA contributes to stress-related hair loss, and ginkgolide A may help treat it.

A 3-year-old girl has a rare condition causing sparse hair and nail issues, with minimal improvement from treatment.

Lizard claws have hair-like keratins similar to those in mammals.

MPZL3 is crucial for seborrheic dermatitis development.

The authors updated the criteria for diagnosing frontal fibrosing alopecia, making it easier to diagnose without a biopsy.

KAP6 genes are conserved across species and active in hair follicles.

Stress can cause a type of hair loss in mice lacking the CCHCR1 gene.

Two siblings have a rare hair condition caused by a new genetic variant.

PPARγ is essential for maintaining healthy skin, controlling inflammation, and ensuring proper skin barrier function.

A person with Werner syndrome was initially thought to just have female pattern hair loss.