Presentation
Presents with history of lethargy, stunted growth, and an abnormal gait.
Patient Data
A poorly-positioned
Case Discussion
The skeletal abnormalities are consistent with congenital hypothyroidism.
thyroxine-t4 * <0.3 (1.1-3.9 UG/DL)
FT4, 2 STEP 0.13 (0.52-1.93 NG/DL)
These changes are indicative of a congenital, developmental or metabolic disease, resulting in underdevelopment of the skeleton and epiphyseal dysplasia, with possible involvement of the abdominal organs.
Differential diagnoses include:
mucopolysaccharoidosis
congenital hypothyroidism
pituitary dwarfism.


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