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Women with Systemic Lupus Erythematosus should have closely monitored pregnancies and avoid certain medications to improve their pregnancy outcomes.

A newborn girl has a rare skin condition with two ulcers on her buttock that are healing on their own.

Mutations in NIPAL4 cause skin issues by disrupting lipid layers, but some improvement is seen with topical treatment.

PCOS is a complex condition in women that can lead to health issues, and lifestyle changes are the best management approach.

Poliosis circumscripta is a patch of white hair caused by lack of melanin, linked to genetic and acquired conditions.

Becker's Nevus Syndrome is a rare condition with a skin patch and possible bone and muscle abnormalities, treated mainly for appearance.

Six genetic conditions are often linked to complete scalp hair loss in children.

Mutations in the Vitamin D receptor gene can cause hair loss similar to mutations in the Hairless gene.

Polycystic Ovary Syndrome (PCOS) is not very common among Iranian women, but it's important to prevent it because of the risk of heart disease and infertility.

Congenital triangular alopecia can occur outside the typical fronto-temporal region.

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

A 17-year-old girl and her brothers have a rare hair condition with long eyelashes, thick eyebrows, and easily pluckable hair.

Early genetic testing and JAK inhibitors can help treat systemic inflammation in SAVI patients.

Early and aggressive treatment is crucial for preserving vision in infants with AEC syndrome.

Hair conditions can be linked to diabetes and affect psychological health.

Conditions affecting sex development show that sexual diversity is a natural part of human variation.

A toddler with a rare adrenal gland tumor causing male-like physical changes was successfully treated with surgery.

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

A man with a rare adrenal cancer showed unusual symptoms and died four months after diagnosis.

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.

A new genetic change causing early stop in the androgen receptor gene was found in a patient with androgen insensitivity syndrome.

A 13-year-old girl was diagnosed with juvenile lupus, showing only hair loss as a symptom.

Sonidegib and vismodegib are similarly effective for advanced basal cell carcinoma, but sonidegib might have a slightly better safety profile.

The document concludes that personalized treatment, including lifestyle changes and medication, is essential for managing PCOS in teenagers, while also addressing their psychological well-being.

An 11-month-old boy with Menkes disease had severe brain shrinkage and abnormal blood vessels, and didn't respond well to treatment.

The document concludes that understanding hair biology and recognizing hair conditions are crucial for managing and treating hair loss in children.

The document concludes that proper diagnosis and management of hair loss in children require a detailed examination and understanding of various hair disorders.

The study found that women with PCOS have more and larger ovarian follicles and differences in ovarian structure, but these features alone can't always diagnose PCOS.

Kids with skin problems are more likely to have mental health issues.

DFMO treatment improves hair growth, muscle tone, and development in Bachmann-Bupp syndrome patients.