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Patients with Shwachman-Diamond syndrome often get misdiagnosed due to a wide range of symptoms, including immune system problems and bone abnormalities.

The document concludes that an inherited nail condition often improves on its own, and spironolactone effectively treats acne in women.

People with myotonic dystrophy type 1 tend to develop basal cell carcinoma at a younger age but not more frequently than others.

A new mutation in the CDH3 gene causes hair loss and vision problems in a young girl.

Oral cyclosporine combined with Pantogar® effectively treats twenty-nail dystrophy.

An 11-year-old Greek girl was diagnosed with a rare genetic disorder, highlighting the importance of genetic testing and family history.

A rare genetic disorder causes sparse hair and vision loss due to a CDH3 gene mutation.

A rare genetic disease causes sparse hair and early blindness due to a gene mutation.

A litter of cats had a hair condition similar to a mouse mutation, leading to hair loss and abnormal hair and skin.

Genetic testing confirmed a rare disorder causing hair loss and vision problems in a Saudi family, stressing its importance for diagnosis and counseling.

Hydroxychloroquine effectively treated twenty-nail dystrophy in a patient with alopecia areata.

Thymoma may link myasthenia gravis, nail dystrophy, and alopecia areata.

Two new mutations in the CDH3 gene cause hair loss and vision problems in a young girl.

Glucocorticoids for progressive muscular dystrophy in children don't improve muscle strength or function but do increase certain side effects.

A genetic mutation in the CDH3 gene causes hair loss and vision problems in a young Saudi girl.

Upadacitinib may effectively treat twenty-nail dystrophy without causing pain.

Ruxolitinib helped a patient with alopecia areata regrow hair.

Antisense oligonucleotides show promise for treating Myotonic Dystrophy type I.

A 10-year-old boy's nail condition is mainly cosmetic and improves over time with treatment.

Cats with abnormal hair had DSG4 gene changes causing hair problems.

A child with rough nails also had hair loss and allergies.

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

Glucocorticoid corticosteroids improve muscle strength in Duchenne muscular dystrophy but can cause side effects.

CRPS type I is a complex pain condition with no proven cure, requiring personalized treatment.

Natural feedstuffs help reduce muscular dystrophy in rabbits more than selenium or vitamin E alone.

A 12-year-old boy with twenty nail dystrophy, a condition affecting all nails, was treated conservatively due to its self-limiting nature and good prognosis.

The review shows that skin symptoms like chronic fungal infections, hair loss, and skin depigmentation are key for early detection and management of APECED.

Annurca apple extract may protect mouse hair from damage by chemotherapy and could help treat hair loss without promoting cancer growth.

A new genetic mutation in the CDH3 gene causes hair loss and eye problems in young people.

CRISPR gene editing reduces harmful molecules in cells from Emery–Dreifuss Muscular Dystrophy patients.