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Consider THPP in patients with muscle weakness and low potassium, as it is often underdiagnosed.

A Persian cat had a rare skin condition that didn't improve with treatment.

Cronkhite-Canada syndrome is rare, with high mortality and cancer risk, needing more research for treatment guidelines.

A patient with Wilson's disease showed hair-pulling behavior as an initial symptom.

Sodium valproate can cause reversible hair loss in some patients.

Certain genetic variants in keratins increase the risk of tooth decay.

Alzheimer's patients have higher levels of certain chemicals in their hair.

Vitamin A toxicity can cause serious health issues like hypercalcemia and is often overlooked.

Valproic acid treatment may cause temporary hair loss due to reduced zinc and biotinidase levels, which tend to normalize after 6 months.

Researchers found a new gene variant linked to a rare bone disease, which doesn't always cause symptoms in carriers.

A woman's rare hair loss condition improved on its own, suggesting this type might recover like common cases.

An 82-year-old man's white hair regained color after taking etretinate for psoriasis.

The document concludes that while white skin, nail, and mucosa diseases increase skin cancer risk, they are generally harmless, especially compared to darker pigmentation conditions.

The document concludes that anticonvulsants like phenytoin may cause skin reactions by affecting tryptophan metabolism and suggests researching vitamin levels in patients with drug reactions.

Cupric chloride treatment corrected abnormal Purkinje cell development in brindled mice.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

About half the patients treated with capecitabine and docetaxel developed severe hand-foot syndrome.

New mutations in hair keratin genes can change hair structure and cause monilethrix, with nail issues more common in certain gene mutations.

Genomic profiling for myeloid cancers can find important inherited mutations, but it's challenging when these mutations aren't related to the patient's symptoms.

People with keratosis pilaris might be more likely to get a rare type of tinea versicolor.

A specific gene mutation causes vitamin D-resistant rickets and hair loss.

A specific gene variation increases the risk of high uric acid and cholesterol in young Mexican males.

Prurigo pigmentosa mainly affects middle-aged White and Asian women, often linked to a ketogenic diet, and is best treated with oral antibiotics.

In 2002, various drugs caused serious side effects, including vitamin B12 deficiency, heart issues, blindness, hypersexuality, allergic reactions, blood clotting problems, pupil dilation, capillary leak syndrome, muscle breakdown, hepatitis, skin reactions, and lupus.

Certain VDR gene changes can affect melanoma risk.

UK medical students lack dermatology education, liver biopsy patients with risk factors show more fibrosis, and certain fungi resist drugs due to melanin; genetics may influence female hair loss.

A patient with a rare hair condition and skin disorder showed hair improvement after treatment.

A baby with a rare metabolic disorder developed a rash not cured by zinc alone, likely due to both zinc and amino acid deficiencies.

Diphencyprone therapy for hair loss can cause vitiligo.