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Adolescents and young adults with Prader-Willi syndrome show a range of sexual interests and behaviors.

Early recognition and multidisciplinary management of Whitaker syndrome can improve patient outcomes.

The woman's facial symptoms are best explained by primary Sjögren’s Syndrome.

High-dose mizoribine effectively controls symptoms in adolescents with lupus while reducing steroid use, with manageable side effects.

Women with hyperandrogenism, especially those with PCOS, are more likely to have psychiatric disorders.

Skin symptoms without a medical cause often reflect psychological stress and are influenced by culture, requiring a team approach for treatment.

A rare hair follicle tumor showed unusual high levels of mucin.

The structured oral exam format is effective and well-received for teaching internal medicine.

A rare case of trichothiodystrophy was found with autism, seizures, and mental retardation.

Different types of skin gland tumors have unique genetic traits, which can guide personalized treatments.

High doses of tryptophan may cause eosinophilic fasciitis.

Young males with severe early-onset hair loss may have a higher risk of metabolic syndrome.

A patient with a new PLEC gene mutation showed symptoms of both muscular dystrophy and myasthenia gravis, which improved with steroid treatment.

The reply suggests checking for false positive or asymptomatic syphilis and using penicillin for treatment if necessary.

The research found that Atypical Progeroid Syndrome has unique symptoms and is not caused by the buildup of a certain mutant protein.

A new HRAS gene variant may cause a range of symptoms including intellectual disability and psychiatric issues.

A patient with Werner syndrome showed a range of aging-like symptoms and metabolic issues, underscoring the need for early detection and treatment.

Trichoscopy can reveal specific hair and scalp changes in linear morphea.

PCOS and related metabolic issues often run in families.

IVIG therapy significantly improved symptoms in a patient with APS-2 and SPS.

Most children with MIS-C showed significant improvement by 6 months.

Most cases of high male hormone levels in women are due to polycystic ovary syndrome.

Myositis in lupus patients is linked to skin rash, hair loss, blood issues, and high disease activity.

Alopecia areata impacts mental well-being more due to perceptions and stigma than disease severity.

Overweight women with PCOS are more likely to have excess male hormones.

Patients with metabolic syndrome had lower Gleason scores when diagnosed with prostate cancer.

A patient with a PLEC mutation has epidermolysis bullosa, muscular dystrophy, and myasthenia gravis, which improved with steroid treatment.

The document describes a rare case of IFAP syndrome, a genetic condition with symptoms of hair loss, light sensitivity, and scaly skin.

Insulin resistance varies among PCOS types, and simple math tools can help identify it early.

A rare genetic mutation causes Woodhouse-Sakati syndrome symptoms.