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Thyroid disorders are common and affect health and quality of life, especially in women, highlighting the need for more awareness and iodine intake.

The study concludes that Loose Anagen Hair Syndrome is a benign condition that usually improves with age but can be hard to diagnose and stressful for the family.

A new mutation in the KRT86 gene causes a hair disorder with variable expression.

A new model helps predict treatment success in girls with early puberty.

A woman with acromegaly experienced severe hair loss from a drug called Lanreotide Autogel, which improved after stopping the treatment.

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

The study found that 7.21% of young girls have polycystic ovarian syndrome, with symptoms like irregular periods, abnormal hair growth, and acne. Early diagnosis is important to prevent long-term complications.

A woman with Kallman's syndrome also developed alopecia universalis, a condition not previously linked to Kallman's.

Olmsted syndrome can be inherited as an autosomal recessive trait due to a rare TRPV3 gene mutation.

A certain gene variation is linked to a higher risk of polycystic ovarian syndrome in South Indian women.

Parry–Romberg Syndrome can involve the brain even without obvious symptoms, and a new diagnostic framework is suggested for early detection.

Two sisters with lipoedematous scalp suggest a genetic influence in the condition.

Cronkhite-Canada syndrome is a rare, non-inherited condition causing various symptoms like polyps, hair loss, and weight loss.

Parental support and gender-affirming care are crucial for the mental health of transgender adolescents.

APS-1 in Italy shows diverse AIRE mutations and various autoimmune issues.

Netherton syndrome causes skin and hair issues, confirmed by "bamboo hair" under dermoscopy, with no cure but managed with topical treatments.

Bardet-Biedl syndrome may include under-recognized skin problems related to its metabolic disturbances.

Surgical removal of abnormal fat pads fixed the woman's eyelid issue caused by likely silicone injections.

Dystonia may be part of PAS-4 and linked to immune issues.

Higher alarin levels might link hair loss and metabolic syndrome.

A child has a rare hair and skin disorder due to specific gene variants, suggesting broader genetic testing is needed.

Treating Netherton syndrome with growth hormone and dupilumab improves growth safely.

A rare genetic mutation causes severe immune issues, hair loss, and nail problems.

A new mutation in the LIPH gene was found to cause a rare hair disorder in a Japanese boy.

Two patients with the same genetic mutation had both blistering skin and easily pulled out hair.

This is the first known case of parathyroid cancer in a patient with Birt Hogg Dube Syndrome.

Turner's syndrome may be linked to autoimmune diseases like psoriasis and alopecia areata, needing comprehensive care.

A boy with long QT syndrome was treated successfully, highlighting the need for careful evaluation of chest pain in children for heart conditions like LQTS.

A new gene mutation causes complete androgen insensitivity in a 16-year-old with a female appearance.

A baby girl has a hair disorder called monilethrix, causing fragile hair that may improve over time.