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Low DHEA-S levels might be linked to alopecia areata and could be a potential treatment target.

Early diagnosis and hormone therapy can significantly improve outcomes for post-partum pituitary insufficiency in resource-limited settings.

Long-term opioid use can cause a serious condition where the adrenal glands don't work properly, which doctors should watch out for.

A woman's severe male hormone excess was caused by a small, hard-to-find ovarian tumor.

Accurate diagnosis of progressive supranuclear palsy requires thorough neurological assessments and MRI.

The woman's rare combination of diseases suggests an unknown factor may predispose individuals to multiple endocrine diseases.

Cronkhite-Canada syndrome causes chronic diarrhea and has a poor prognosis despite treatment.

Pseudopelade of Brocq is a unique hair loss condition, but its cause and development are still not fully understood.

Recognizing the link between certain autoimmune disorders and neurological conditions can improve diagnosis and treatment.

Affected males are born with ambiguous genitalia, raised as females, but develop male traits at puberty due to enzyme deficiency.

Hair loss in Cronkhite-Canada syndrome is reversible by treating the gut issues and doesn't need steroid treatment for the hair itself.

COVID-19 and hypopituitarism (reduced pituitary gland function) are linked, with the latter's related health issues potentially worsening COVID-19 outcomes, and COVID-19 possibly increasing risk for pituitary complications.

Long-term treatment with buprenorphine/naloxone for opioid addiction may lead to secondary adrenal insufficiency.

Trilostane treatment led to full hair regrowth in most Pomeranians and all miniature poodles with alopecia X.

Certain factors can trigger hormonal imbalances and cyst formation, leading to Polycystic Ovarian Syndrome (PCOS).

PCOS patients have higher LDH and lower cortisol, dopamine, zinc, and vitamin D3, which may contribute to their symptoms and obesity.

Men might have a version of the female disease, polycystic ovarian syndrome, shown by changes in hormone levels and early baldness, but more research is needed to fully understand it.

Timely diagnosis and treatment of complex autoimmune diseases like APS2 are crucial to prevent complications and improve life quality.

A woman's hair loss and other symptoms were due to a rare hormone deficiency treatable with steroids.

Late diagnosis of congenital adrenal hyperplasia can greatly affect physical development, gender identity, and sexual health.

Early recognition and tailored treatment are crucial for managing overlapping systemic lupus erythematosus and systemic sclerosis.

A young woman had a rare, aggressive ovarian tumor that was hard to diagnose and treat, leading to disease progression despite treatment.

Acne is a chronic disease linked to various systemic conditions and has significant psychological and social effects.

The patient with lupus and Degos' disease showed significant improvement with treatment.

Early diagnosis and treatment of NCCAH can improve symptoms and fertility.

A pancreatic tumor caused high glucagon levels and symptoms, but treatment reduced glucagon and shrank liver tumors.

Hidradenitis suppurativa is linked to various diseases like obesity, depression, arthritis, and Crohn's disease, but often occurs alone.

Pimozide treatment resolved cysts and partially restored cheek fat in a man with Barraquer–Simons syndrome.

The man had pretibial myxedema and hyperthyroidism, causing skin changes and thyroid issues.

A woman with a specific mutation causing adrenal gland issues faced fertility problems, but careful hormone therapy helped her manage it successfully.