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A 4-year-old boy with a rare type of rickets and hair loss improved in bone health but not hair growth after vitamin D and calcium treatment.

RSPO1 mutations in certain patients lead to skin cells that don't develop properly and are more likely to become invasive, increasing the risk of skin cancer.

Dermoscopy helped diagnose a rare hair disorder in a 2-year-old boy.

Cyclosporine-A can cause excessive hair growth, which usually stops after discontinuing the drug.

The patient was diagnosed with oral lichen sclerosus and needs long-term monitoring.

Erythromelanosis follicularis faciei can also affect women, though it's rare.

Frizzled 3 and Frizzled 6 together control the orientation of mouse hair follicles.

Leptin-deficient mice, used as a model for Type 2 Diabetes, have delayed wound healing due to impaired contraction and other dysfunctional cellular responses.

Narrowband UVB therapy significantly improved a child's rare skin condition.

Laser hair removal is effective for hirsutism when combined with treatment for the underlying causes.

Bone marrow stem cells and their medium help hair regrowth.

In India, most patients with type 1 autoimmune polyglandular failure show symptoms in a specific order, starting with parathyroid gland issues, then yeast infections, and finally adrenal gland failure.

Human hair keratins K85 and K35 create unique filament patterns important for early hair formation.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

The girl has both monilethrix and Type 1 diabetes, but no link between the two conditions is known.

Gemstones are used to help describe and remember skin conditions.

CaBP1 and CaBP2 are necessary for proper hearing and neurotransmission in the ear's inner hair cells.

CaBP1 and 2 are important for maintaining the activity of calcium channels necessary for hearing in inner ear cells.

Androgen treatment with dihydrotestosterone may help maintain height in patients with 5-α-reductase type 2 deficiency, especially before puberty.

A baby with a skin condition improved with treatment but developed a rare form of the condition affecting only his trunk.

A man with itchy skin lesions and weight loss was diagnosed with a rare skin condition linked to a pancreatic tumor.

Frizzled receptors are essential for various body development processes and maintaining certain body functions.

Primary cicatricial alopecia, a rare disorder causing permanent hair loss, is hard to diagnose and treat, with treatments like anti-inflammatory drugs and steroids offering varied results and no guaranteed cure. Psychological support for patients is important, and future research should aim to identify causes of the condition.

sPLA2-IIE is crucial for normal hair follicle structure and skin health.

English springer spaniels are more prone to severe sebaceous adenitis than standard poodles.

EGFR helps control how hair grows and forms without needing p53 protein.

The document reports a unique case of woolly hair with a combination of conditions not previously seen together.

A woman with lupus had muscle weakness due to kidney issues and was successfully treated with medication.

People with Epidermolysis bullosa have many health problems including poor oral health, which is often neglected due to other medical issues.