Cretinism history and symptoms: Difference between revisions

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==Overview==
==Overview==
The majority of patients with [disease name] are asymptomatic.
The majority of patients with cretinism are asymptomatic. A positive history of a family member had the disease before and maternal history of thyroid problems is suggestive of cretinism. The most common symptoms of cretinism include [[lethargy]], [[hoarse]] cry, [[constipation]], and [[umbilical hernia]]. Less common symptoms of cretinism include [[Palpation|palpable]] [[goiter]].
OR
The hallmark of [disease name] is [finding]. A positive history of [finding 1] and [finding 2] is suggestive of [disease name]. The most common symptoms of [disease name] include [symptom 1], [symptom 2], and [symptom 3]. Common symptoms of [disease] include [symptom 1], [symptom 2], and [symptom 3]. Less common symptoms of [disease name] include [symptom 1], [symptom 2], and [symptom 3].


Infants born in regions of the world that lack newborn screening programs are more likely to present with symptoms and signs of congenital hypothyroidism, which include lethargy, hoarse cry, feeding problems, often needing to be awakened to nurse, constipation, puffy (myxedematous) facies, macroglossia, umbilical hernia, large fontanels, hypotonia, dry skin, hypothermia, and prolonged jaundice. A few newborn infants with thyroid dyshormonogenesis have a palpable goiter at presentation, while in others the goiter is discovered later in life.
==History and Symptoms==
==History and Symptoms==
* Patients with cretinism may be asymptomatic at the beginning.
* History taking is essential in suspected cases of cretinism:
** Family history should be asked to detect any [[genetic inheritance]] among the family members. 
** Maternal history should be also taken to detect if the mother had any thyroid problems before and to inform about the pregnancy. 
===Common Symptoms===
===Common Symptoms===
Common symptoms of [disease] include:
Common symptoms of cretinism include:<ref name="pmid9579233">{{cite journal| author=Law WY, Bradley DM, Lazarus JH, John R, Gregory JW| title=Congenital hypothyroidism in Wales (1982-1993): demographic features, clinical presentation and effects on early neurodevelopment. | journal=Clin Endocrinol (Oxf) | year= 1998 | volume= 48 | issue= 2 | pages= 201-7 | pmid=9579233 | doi= | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=9579233  }}</ref>
*[symptom 1]
*[[Lethargy]]
*[symptom 2]
*[[Hoarse]] cry
*[symptom 3]
*[[Constipation]]
*[[Myxedematous]] facial features
*[[Umbilical hernia]]


===Less Common Symptoms===
===Less Common Symptoms===
Less common symptoms of [disease name] include  
Less common symptoms of cretinism include  
*[symptom 1]
*[[Palpable]] [[goiter]]
*[symptom 2]
*[symptom 3]


==References==
==References==
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​​[[Category:Medicine]]
[[Category:Endocrinology]]
[[Category:Up-To-Date]]​
[[Category:Pediatrics]]

Latest revision as of 20:37, 27 October 2017

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ahmed Elsaiey, MBBCH [2]

Overview

The majority of patients with cretinism are asymptomatic. A positive history of a family member had the disease before and maternal history of thyroid problems is suggestive of cretinism. The most common symptoms of cretinism include lethargy, hoarse cry, constipation, and umbilical hernia. Less common symptoms of cretinism include palpable goiter.

History and Symptoms

  • Patients with cretinism may be asymptomatic at the beginning.
  • History taking is essential in suspected cases of cretinism:
    • Family history should be asked to detect any genetic inheritance among the family members.
    • Maternal history should be also taken to detect if the mother had any thyroid problems before and to inform about the pregnancy.

Common Symptoms

Common symptoms of cretinism include:[1]

Less Common Symptoms

Less common symptoms of cretinism include

References

  1. Law WY, Bradley DM, Lazarus JH, John R, Gregory JW (1998). "Congenital hypothyroidism in Wales (1982-1993): demographic features, clinical presentation and effects on early neurodevelopment". Clin Endocrinol (Oxf). 48 (2): 201–7. PMID 9579233.

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