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

Finasteride significantly reduced tics and obsessive-compulsive symptoms in Tourette syndrome patients.

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.

A woman's progressive hair loss was correctly diagnosed as a rare condition called fibrosing alopecia in a pattern distribution after initially being mistaken for a more common type.

A 15-year-old boy's skin and hair condition worsened due to improper treatment, leading to severe health issues.

Patients with central centrifugal cicatricial alopecia may have a higher risk of breast and colorectal cancer.

A young woman with a rare fungal infection showed significant improvement after treatment with antifungal medication.

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

A patient with Alopecia Areata had complete hair regrowth after using the drug baricitinib.

A boronic acid copolymer quickly forms cell clusters, useful for tissue and tumor modeling.

Clouston's syndrome is a rare disorder affecting nails, hair, teeth, and skin, caused by a gene mutation, and currently has no treatment, only supportive care.

Hydrogel surface properties affect mouse embryoid body differentiation.

High selenium levels in some areas cause health issues in cows and buffaloes, but blood tests remain normal.

Netherton's syndrome may have a familial link and doesn't always include atopy.

A 33-year-old woman with PCOS and metabolic syndrome was unusually diagnosed with a bone condition called DISH, suggesting a possible link between these conditions.

Radiological findings help distinguish LAM, PLCH, and BHD to avoid invasive tests.

Clouston syndrome causes issues with teeth, hair, nails, and skin, and has no cure, but recognition has improved.

Basal cell carcinomas need extra mutations to grow from small to large tumors.

Early diagnosis and treatment of haemochromatosis are crucial for reversing organ damage and improving fertility.

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

Skin lesions in Carney Complex are caused by a gene change in some skin cells that leads to increased pigmentation and may lead to tumors.

BLMP-1 is important for regular molting and gene expression cycles in worms.

A man with a rare disease experienced late hair whitening and loss, but hair color returned, suggesting a good outlook.

The research found that a protein called caveolin-1 is reduced in psoriasis, but reintroducing it can help alleviate some psoriasis symptoms.

Polyamines are crucial for skin tumor development, and inhibiting them can prevent tumors.

A new medical syndrome may include skin changes, hair loss, sweating issues, bone malformations, leg swelling, and low cortisol.

An 8-year-old boy with hair-pulling disorder had a bald patch that was confirmed not to be a fungal infection and was treated with therapy.

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 development of breeding tubercles in male zebrafish relies on a specific enzyme that processes hormones.

A new genetic mutation was found causing hair and eye issues in a boy.