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A 17-year-old girl had severe, on-and-off hair loss, likely due to COVID-19. She was treated with Vitamin D3, biotin, and other supplements, and saw some improvement within a month.

A girl with a rare skin condition improved after one month of treatment with acitretin.

A new MTX2 gene mutation caused a severe genetic disorder in a young Chinese girl.

Acrodermatitis enteropathica is a rare inherited disorder causing skin issues, diarrhea, and hair loss.

Two siblings had a rare immune disorder caused by a FOXN1 gene mutation.

Trilostane effectively improved symptoms in dogs with a certain adrenal gland disorder.

A Korean boy's skin and digestive symptoms were caused by a rare genetic disorder that affects zinc absorption, and he got better with zinc supplements.

A boy with chromosome 13q deletion syndrome developed eye cancer, a woman with breast cancer lost vision due to a rare side-effect of her treatment, a man's vision worsened after using a hair loss drug, and two rare disorders were discussed. Optical Coherence Tomography is useful for diagnosing and monitoring these conditions.

The document discusses various eye conditions and their treatments, including a rare eye cancer in a baby, vision loss from a cancer drug, cataracts from a baldness treatment, a rare skin disorder, and a specific type of eye disease diagnosed with a special imaging technique.

The new gel formula could improve the delivery of a hair loss treatment through the skin and might be an alternative to taking it by mouth.

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

Zinc supplements improved the girl's skin and hair condition.

A young Russian girl with Meier-Gorlin syndrome has two new mutations in the CDC6 gene.

The rash on the infant indicated a serious underlying condition.

Oral isotretinoin temporarily improved skin symptoms in a child with IFAP syndrome.

Accurate diagnosis and zinc supplements can improve life quality in acrodermatitis enteropathica, even with normal zinc levels.

A genetic defect in an Appenzeller Mountain Dog caused skin issues, improved with ketoconazole, showing the importance of advanced genetic testing.

A child with skin and tooth symptoms was found to have a genetic mutation causing cardiocutaneous syndrome, leading to heart problems.

Early genetic testing and zinc therapy are crucial for managing acrodermatitis enteropathica effectively.

Early genetic testing and zinc therapy are crucial for managing acrodermatitis enteropathica in infants.

Early diagnosis and treatment of hereditary vitamin D-resistant rickets (HVDRR) are crucial to prevent growth issues and other health problems.

Netherton syndrome can cause severe dehydration, infections, and growth issues in infants.

A woman's eyelashes grew thicker and longer after taking topiramate, but returned to normal when she stopped the medication.

Hypertrichosis (excessive hair growth) can help diagnose superficial epidermolytic ichthyosis.

An infant with seizures and hair loss was diagnosed with biotinidase deficiency and treated successfully with biotin.

Platelet-rich plasma is a promising and safe treatment for increasing hair density and thickness in women with chronic telogen effluvium.

An 11-year-old girl with compulsive hair pulling was successfully treated with therapy and medication.

Biotinidase deficiency can mimic other conditions, making early diagnosis and treatment crucial to prevent lasting issues.

A child with rickets and hair loss might have a rare type of rickets that doesn't improve much with usual vitamin D and calcium treatment.

AE can have varied symptoms and genetic causes, but zinc therapy helps.