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A child was initially wrongly diagnosed with a fungal scalp infection but actually had a non-scarring hair loss condition called Temporal Triangular Alopecia.

The conclusion is that the variation in hair thinness in patients is mostly due to the amount of underdeveloped hairs, and treatments that thicken fine hairs might work for those with mild to severe conditions.

Recurrent pneumothorax can occur in Sjogren's syndrome, even without common markers.

Cognitive-behavioral therapy with habit reversal training is the most effective treatment for trichotillomania.

Mutations in the ST14 gene cause skin and hair issues by disrupting important protein processing.

Mutations in the DSG4 gene cause fragile, sparse hair in humans, mice, and rats.

Reptiles on the Absheron Peninsula accumulate toxic elements in their tissues but survive due to tissue resilience.

A new syndrome, Teelwani Syndrome, combines features of two rare genetic disorders.

Skin tumor cells in patients with tuberous sclerosis have higher levels of a protein called cathepsin B.

The document reports unique growth lines in a child after Stevens-Johnson syndrome, skin reaction from parsnips and sun in a girl, and itchy skin with xanthomas in a boy with Alagille syndrome.

Cathepsin L deficiency causes hair and skin issues in mice.

Trichotillomania can be identified by a "Friar Tuck sign" and nail-biting.

Monilethrix hair issues are due to problems in the hair's internodes.

Polarizing light microscopy can easily and reliably diagnose congenital keratinizing disorders like Netherton syndrome.

Ultrasound effectively distinguishes trichilemmal cysts from epidermoid cysts.

Care for gender-dysphoric Veterans can be improved with a consistent, team-based approach.

A specific gene mutation causes hair loss and potential eye issues, even if vision seems normal.

Tofacitinib helps improve skin conditions in people with Down syndrome, especially alopecia areata.

Recognizing both trichostasis spinulosa and eruptive vellus hair cysts together is crucial for accurate diagnosis and treatment.

Trps1 plays a key role in hair follicle development and cycling.

The meeting highlighted the complexity and variability of skin conditions and differing opinions on their diagnoses and treatments.

New compounds were made that block an enzyme linked to breast cancer better than existing treatments.

Milia, SM, and EVHC may be related conditions, not separate ones.

The method allows detailed observation of hair tissue structures.

Successful outcomes depend on accurate diagnosis and strong doctor-patient relationships.

N-acetylcysteine may help treat trichotillomania.

Trichoscopy helps tell apart hair loss due to alopecia areata from trichotillomania in eyebrows.

Teprotumumab for thyroid eye disease commonly causes fatigue, brittle nails, dry eyes, hair loss, muscle spasms, and dry mouth, with rare serious events like blood clots.

Five different TPO gene mutations were found in PCOS patients with thyroid hormone issues.