Pediatric endocrinology through syndromes

Eur J Med Genet. 2020 Jan;63(1):103614. doi: 10.1016/j.ejmg.2019.01.004. Epub 2019 Jan 14.

Abstract

In everyday practice, a pediatric endocrinologist will face a variety of different endocrine issues (such as short or tall stature, dysthyroidism, abnormal pubertal timing or impaired glucose metabolism), which relevantly contribute to the global care of a number of syndromic conditions. On the other hand, the presence of endocrine features may assist in the diagnostic process, leading to final diagnosis of a syndromic disorder. The intention of this review is to provide a referenced overview of different genetic syndromes characterized by endocrine features, and to present a possible classification, based on whether the endocrinopathy or the syndrome is typically recognized first. Thus, the first part of the manuscript deals with the most common syndromes associated with endocrine dysfunctions, while the second part describes the conditions by which a syndrome is most frequently diagnosed after an endocrine finding. The aim is to provide a practical overview of the assessment of syndromic patients, so that they can be recognized and managed in an integrated, multidisciplinary fashion.

Keywords: Diabetes; Puberty; Stature; Syndrome; Thyroid.

Publication types

  • Review

MeSH terms

  • Body Height / genetics
  • Child
  • Endocrine System Diseases / genetics*
  • Endocrine System Diseases / metabolism
  • Endocrine System Diseases / pathology
  • Endocrinologists
  • Growth Disorders / epidemiology
  • Growth Disorders / genetics*
  • Growth Disorders / pathology
  • Human Growth Hormone / genetics*
  • Human Growth Hormone / metabolism
  • Humans
  • Pediatrics / trends

Substances

  • Human Growth Hormone