File:Congenital hypothyroidism.jpg

From Embryology

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Infant with Congenital Hypothyroidism

Typical appearance of a hypothyroid infant before the advent of newborn screening is shown in the infant.

A - 3 month old infant with untreated CH; picture demonstrates hypotonic posture, myxedematous facies, macroglossia, and umbilical hernia.

B - Same infant, close up of face, showing myxedematous facies, macroglossia, and skin mottling.

C - Same infant, close up showing abdominal distension and umbilical hernia.


Rastogi and LaFranchi Orphanet Journal of Rare Diseases 2010 5:17 doi:10.1186/1750-1172-5-17

Reference

<pubmed>20537182</pubmed>| Orphanet J Rare Dis.


© 2010 Rastogi and LaFranchi; licensee BioMed Central Ltd. This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.

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current13:56, 23 July 2010Thumbnail for version as of 13:56, 23 July 2010600 × 481 (51 KB)S8600021 (talk | contribs)==Infant with congenital hypothyroidism== Typical appearance of a hypothyroid infant before the advent of newborn screening is shown in the infant. A - 3 month old infant with untreated CH; picture demonstrates hypotonic posture, myxedematous facies, ma

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