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Aire mutation reduces alopecia areata, while Notch4 mutation prevents it in mice.

A woman had a skin condition with increased normal elastic fibers, not related to other known disorders, likely due to aging.

Scientists found a gene in mice that causes early hearing loss.

AIRE-deficient rats developed severe autoimmune disease similar to APECED, useful for testing treatments.

Latanoprost, a glaucoma medication, caused excessive eyelid hair growth in many patients.

Elderly patients with CCCA were all African American with low vitamin D, but no iron or zinc deficiencies, and no hormonal imbalances compared to younger patients.

Aging-related hormone changes affect voice quality, especially during puberty, menstruation, pregnancy, and menopause.

Barn owls with smaller black spots have higher testosterone levels, which might be due to genetic effects on hormone regulation rather than hormone effects on coloration.

A new method accurately predicts the flight path of unguided projectiles.

Becker's Melanosis and Hypertrichosis mainly affects young males, causing brown skin patches and extra hair on one side of the upper body.

A woman with acromegaloidism and normal growth hormone levels had a rare X-Tetrasomy, suggesting a need to study X-chromosome genes for their role in growth and facial development.

Skin lesions in Carney complex are likely caused by a specific group of skin cells that promote pigment production due to a genetic mutation.

The boy's symptoms suggest a possible new medical condition.

A rare genetic mutation caused unusual skin symptoms in a man with Blau syndrome.

A woman with Hashimoto's hypothyroidism developed Graves' hyperthyroidism after 20 years, showing these conditions may be linked.

The two-factor model fits better for Chinese patients' understanding of illness causes than the original four-factor model.

Fibrosing alopecia in a pattern distribution is a type of hair loss that may often be overlooked, especially in men.

Young patients with Vogt-Koyanagi-Harada syndrome may have poor vision outcomes despite treatment due to frequent recurrences.

ODC overexpression in hair cells increases tumor growth by reducing Notch signaling.

A woman's masculine symptoms were caused by a rare tumor in her left ovary, which was found using a special blood test.

The symptoms described align more with Haberland syndrome, not Delleman-Oorthuys syndrome.

Most patients with chronic hair shedding did not progress to permanent hair loss, and one showed improvement with treatment.

Lithium can cause skin changes similar to mycosis fungoides.

Dermoscopy helps dermatologists diagnose different types of hair loss accurately without always needing a biopsy.

Dystonia may be part of PAS-4 and linked to immune issues.

Bird foot scales develop differently and can repair but not fully regenerate due to the lack of specialized stem cell areas.

A 10-year-old girl with hair and eyelash loss showed significant regrowth after treatment.

Kainar syndrome symptoms may be linked to nuclear test exposure effects.

Finasteride treatment increased blood volume and reduced vessel leakiness in beagle prostates.

A 6-year-old boy with autism improved his thyroid function and growth after addressing iodine deficiency caused by picky eating, but his psychiatric symptoms and picky eating continued.