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Erosive palmoplantar lichen planus in North-East India mainly affects the feet and often involves nails, with unique inflammatory skin changes.

New treatments targeting specific genes show promise for treating keratin disorders.

The naked mutation in mice causes hair loss and helps identify keratin genes.

Valproic acid can very rarely cause nail separation, which usually gets better on its own after stopping the drug.

Hair-tourniquet syndrome can cause serious toe injuries in infants but can be treated if found early.

Naked-mouse hair lacks certain proteins and has less soluble fibril.

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

Monilethrix is linked to a gene cluster on chromosome 12.

The patient's hair was thinner and had fewer lipids due to a genetic mutation.

Hair shaft dysplasias are abnormal hair conditions that can be inherited or acquired and may signal other health issues, with limited treatment options available.

Tiger tail banding and hair abnormalities are reliable indicators for diagnosing trichothiodystrophy.

The lanceolate hair-J mutation in mice helps understand human hair disorders like Netherton's syndrome.

Early diagnosis and a multidisciplinary approach are crucial for children with Trichothiodystrophy and hidden learning disorders.

Povidone-iodine nail solution effectively treats nail infections caused by chemotherapy.

Trichothiodystrophy is a rare genetic disorder causing hair issues and sometimes linked to DNA repair defects.

Trichorrhexis nodosa is common hair breakage, often due to styling, and new treatments are being explored.

Fragile hair in children is rarely linked to trichothiodystrophy (TTD).

A rare skin condition in a baby showed unusual fat and hair follicle changes.

Smoking and certain health conditions like thyroid disease may make palmoplantar pustulosis harder to treat.

Most patients with Porphyria Cutanea Tarda had skin blisters and were often affected by hepatitis C and alcohol abuse, with differences between familial and sporadic cases.

Consider necrolytic acral erythema in similar cases and treat with oral zinc sulfate.

A woman with myotonic dystrophy had multiple skin tumors on her scalp, suggesting a genetic link.

MRI can show unusual brain changes in adrenomyeloneuropathy.

Monitor for early signs of azathioprine toxicity and check blood counts regularly.

Pili torti is a rare condition where hair is twisted and breaks easily, often linked to genetic disorders or other health issues.

Tissue-specific variation in mutant load complicates genetic counseling and prenatal diagnosis.

Tofacitinib improved hair and nail conditions in a teen with alopecia areata.

A patient with steroid sulfatase deficiency had a unique hair pattern and a brain malformation not previously linked to the condition.