Failure to thrive (FTT) is not a diagnosis but a sign of inadequate nutrition in young children manifested by a failure of physical growth, usually affecting weight. In severe cases,...
Successful treatment of FTT almost always is accomplished by a careful and detailed history because most cases are due to underfeeding or inappropriate feeding.
Prenatal and developmen...
Treat underlying conditions.
Caregiver and infant interaction should be evaluated in infants and children with FTT.
Age-appropriate nutritional counseling should be provided (1...
If specific disease is identified, follow up as indicated.
Close (every 2–4 weeks at first, then 1–2 months if good progress), long-term follow-up with frequent vi...
Atalay A, McCord M. Characteristics of failure to thrive in a referral population: implications for treatment. Clin Pediatr (Phila). 2012;51(3):219–225. [View Abstract on Ovid...
R62.51 Failure to thrive (child)
P92.6 Failure to thrive in newborn
783.41 Failure to thrive
779.34 Failure to thrive in newborn
54840006 Failure to thrive (disorder)
433476000 failure...
FTT is a sign of inadequate nutrition. It is rarely due to a medical condition.
Underlying medical and/or social issues are generally suggested by history and physical exam, and extensi...
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<bold>FIGURE 7-7</bold> Turner syndrome. Short stature, stocky build, crest chest, lack of breast development, and cubitus valgus are evident in this 13-year-old girl.
<bold>FIGURE 7-7</bold> Turner syndrome. Short stature, stocky build, crest chest, lack of breast development, and cubitus val...
<bold>FIGURE 38-1.</bold> In irritable bowel syndrome ( IBS) , the spastic contractions of the bowel can be seen on x-ray contrast studies.
<bold>FIGURE 38-1.</bold> In irritable bowel syndrome ( IBS) , the spastic contractions of the bowel can be seen on x-ray cont...
A. Translocation of the long arms of chromosomes 14 and 21 at the centromere. Loss of the short arms is not clinically significant, and these individuals are clinically normal, although they are at risk for producing offspring with unbalanced translocations. B. Karyotype of translocation of chromosome 21 into 14, resulting in Down syndrome.
A. Translocation of the long arms of chromosomes 14 and 21 at the centromere. Loss of the short arms is not clinically significant, and th...
Trisomy 21 in the karyotype of a child with Down syndrome. All other chromosomes are normal.