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A new severe form of monilethrix syndrome includes hair loss, scalp itching, cataracts, and distinct facial features.

A boy with Sjogren-Larsson syndrome has skin and muscle symptoms due to a specific enzyme deficiency.

Classical PCOS types A and B are most common and linked to higher health risks.

Health care providers should address the emotional challenges of SLE patients with comprehensive care.

scINSIGHT accurately identifies cell clusters and gene patterns in complex data.

Tislelizumab can cause cutaneous lupus erythematosus.

SOCS1 and SOCS3 help control skin inflammation and are important for developing treatments for skin diseases.

The case shows skin changes can indicate deeper health issues like insulin resistance, which are challenging to manage.

The NIPAL4 mutation c.527C>A is common in Romanian patients with autosomal recessive congenital ichthyosis.

A unique gene mutation was found in a family with monilethrix.

Ayurvedic treatments successfully helped two women with infertility have healthy pregnancies.

A woman was the first known case to have both polycystic ovary syndrome and autoimmune polyglandular syndrome type 2, suggesting a need to check for both conditions in similar patients.

Syphilis can cause hair loss that looks like other conditions, but it improves with treatment.

Certain immune system genes are linked to a higher risk of psoriasis and psoriatic arthritis, while others may offer protection.

The Society had a promising start to 2021 with a new online platform, grants program, and elected Trustees.

CAM practitioners in the eThekwini area are exploring ways to manage and diagnose Polycystic Ovarian Syndrome.

PSA levels are higher in women with PCOS, but FAI is a more accurate marker for diagnosis.

Nagashima-type palmoplantar keratosis in Asians is caused by a SERPINB7 gene mutation.

9-cis-retinoic acid showed some effectiveness in treating AIDS-related Kaposi sarcoma but had significant side effects at higher doses.

Thorough history and examination are crucial for diagnosing genetic disorders like juvenile polyposis and hypomelanosis of Ito.

A young patient with unusual insulin resistance and high testosterone levels had a rare INSR gene mutation.

A patient had both white piedra and head lice, showing their differences.

Early diagnosis and treatment are crucial for complex medical conditions.

A rare skin condition was confirmed to be associated with a specific virus in a young girl.

Recessive X-linked ichthyosis involves a less efficient enzyme in hair follicles, suggesting two distinct enzymes.

A 5-year-old girl has lipoid proteinosis, causing voice issues, hair thinning, skin lesions, and tongue movement problems.

The report expanded knowledge of MBTPS1-related disorders by identifying new symptoms.