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Froelich syndrome
Other Resources UpToDate PubMed

Froelich syndrome

Other Resources UpToDate PubMed

Synopsis

A rare endocrine disorder that is characterized by obesity, hypogonadism, and growth retardation. Due to changes in secondary sex characteristics that result from the impaired function of hypothalamic neurons that regulate pituitary hormone secretion and energy homeostasis. Commonly seen in those with sella tumors or hypothalamic lesions.

Patients exhibit hyperphagia, polydipsia, and polyuria. Thought to be acquired, and appears in males more frequently than in women.

Distinguish between primary hypogonadism and secondary hypogonadism for accurate diagnosis. Can resemble the genetic disorder Prader-Willi syndrome.

Codes

ICD10CM:
E23.6 – Other disorders of pituitary gland

SNOMEDCT:
62999006 – Adiposogenital dystrophy

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Last Updated:09/09/2015
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Froelich syndrome
A medical illustration showing key findings of Froelich syndrome : Vision loss
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