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No endocrinopathy has been described.
Exists the possibility that this defect depends on a moniliasis (candidiasis, candida endocrinopathy syndrome).
Mitochondrial disorders often present themselves as neurological disorders, but can manifest as myopathy, diabetes, multiple endocrinopathy, or a variety of other systemic manifestations.
The etiology can be psychological stress, weight (obesity, anorexia, or a rapid change), exercise, endocrinopathy, neoplasm, drugs, or it may be otherwise idiopathic.
Failure to make this transition smoothly should raise suspicion of insufficient glucocorticoid supplementation, concurrent endocrinopathy (e.g. hypothyroidism), or cocurrent illness (especially renal damage).
Endocrinopathy: In women, amenorrhoea, and in men, gynaecomastia, erectile dysfunction and testicular atrophy, are common early symptoms due to dysfunction of the gonadal axis.
Other conditions with similar presentations include: bacterial folliculitis and demodicosis, dermatophytosis, endocrinopathy, pemphigus foliaceus, Zinc responsive dermatosis, vitamin A-responsive dermatosis, ichthyosis, and nutritional deficiencies.
See main article at Endocrine diseases A disease due to a disorder of the endocrine system is often called a "hormone imbalance", but is technically known as an endocrinopathy or endocrinosis.
Satoyoshi syndrome, also known as Komura-Guerri syndrome, is a rare progressive disorder of presumed autoimmune etiology, characterized by painful muscle spasms, alopecia, diarrhea, endocrinopathy with amenorrhoea and secondary skeletal abnormalities.
POEMS syndrome - the E is for endocrinopathy; the cause is a paraprotein excreted by a plasmacytoma or multiple myeloma; other features are polyneuropathy, organomegaly (hepatomegaly and splenomegaly), M-protein (paraprotein) and skin changes.
The IPEX syndrome is characterized by the development of overwhelming systemic autoimmunity in the first year of life, resulting in the commonly observed triad of watery diarrhea, eczematous dermatitis, and endocrinopathy seen most commonly as insulin-dependent diabetes mellitus.
MEN1 should be suspected in patients with an endocrinopathy of two of the three characteristic affected organs, or with an endocrinopathy of one of these organs plus a first-degree relative affected by MEN1 syndrome.
Acanthosis nigricans associated with obesity, insulin-resistant states, and endocrinopathy (also known as "Acanthosis nigricans type III") is the most common variety of acanthosis nigricans, presenting with a grayish, velvety thickening of the skin on the sides of the neck, axillae, and groins.