Management of a 6-Month-Old Infant with Severe Growth Failure (0th Percentile Height)
Immediate priority is aggressive nutritional optimization with high-calorie, high-protein feeding (130 kcal/kg/day, 4 g/kg protein/day), delivered via nasogastric tube or gastrostomy if oral intake is insufficient, as this represents the most critical and reversible cause of growth failure in infancy. 1
Initial Diagnostic Workup
The evaluation must systematically exclude treatable causes before considering any hormonal interventions:
Essential Laboratory Testing
Metabolic panel: Screen for chronic kidney disease, electrolyte disturbances (hyponatremia), metabolic acidosis (bicarbonate <22 mEq/L), and dehydration—all of which severely impair infant growth 1
Thyroid function: Measure TSH and free T4 to identify hypothyroidism, which is a completely reversible cause of growth failure and must be treated before any other intervention 1
Renal function: Obtain serum creatinine and estimated GFR, as chronic kidney disease is a major cause of infant growth failure 1
Nutritional markers: Check albumin, calcium, phosphorus, alkaline phosphatase, 25-hydroxyvitamin D3, and parathyroid hormone to identify mineral dysregulation and nutritional deficiencies 1
Celiac screening: Tissue transglutaminase IgA with total IgA, as celiac disease can present with isolated growth failure 2
Complete blood count: Screen for chronic anemia suggesting inflammatory bowel disease or nutritional deficiency 2
Genetic Evaluation
Karyotype analysis: Mandatory in all female infants with severe short stature to rule out Turner syndrome, which is the most commonly missed pathologic diagnosis 2
Skeletal survey: Assess body proportions for skeletal dysplasia if disproportion is noted 2, 3
Nutritional Management (First-Line Intervention)
Infancy represents the most nutrition-sensitive phase of growth, and optimal nutritional management can result in catch-up growth even in severe chronic kidney disease. 1
Specific Nutritional Requirements
Energy: 130 kcal/kg/day 1
Protein: 4 g/kg/day 1
Salt restriction: <0.5 g/day for infants <6 months 1
Delivery method: Enteral tube feeding or gastrostomy must be considered if oral intake is insufficient—fluid restriction should never compromise caloric intake 1
Expert dietician involvement: Mandatory for structured meal planning and monitoring 1, 2
Correction of Metabolic Derangements
Metabolic acidosis: Correct to bicarbonate ≥22 mEq/L with sodium bicarbonate supplementation 1
Electrolyte replacement: Provide free water and sodium supplementation if hyponatremia and polyuria are present to avoid chronic intravascular volume depletion 1
Vitamin D and calcium: Supplement with cholecalciferol or calcifediol plus calcium (250-500 mg/day) if ionized calcium is low or PTH is elevated 1
Secondary hyperparathyroidism: Control marked elevations before considering growth hormone therapy 1
Growth Hormone Therapy Considerations
Growth hormone should NOT be initiated until nutritional deficiencies and metabolic derangements are adequately corrected. 1
Criteria for Growth Hormone Therapy at 6 Months
Growth hormone may be considered at 6 months of age ONLY if ALL of the following criteria are met:
Estimated GFR ≤60 ml/min/1.73 m² (if chronic kidney disease is present) 1
Nutritional deficiencies have been excluded and corrected 1
Metabolic acidosis has been corrected 1
Hypothyroidism has been excluded or treated 1
Pre-Treatment Assessments Before Growth Hormone
If growth hormone therapy is being considered, the following must be completed:
Fundoscopic examination: Rule out papilledema (absolute contraindication) 1, 5
Bone age radiograph: Left wrist X-ray to confirm open epiphyses and assess growth potential 1, 5
IGF-1 levels: Baseline measurement 1
Fasting glucose and HbA1c: Screen for glucose abnormalities 1
Growth Hormone Dosing (If Indicated)
Timing: Evening administration 4
For chronic kidney disease: Weekly dosage up to 0.3 mg/kg divided into daily injections 6
Monitoring Strategy
Height measurements: Every 3 months in infants to calculate growth velocity 2, 7
Growth velocity assessment: Persistently reduced growth rate beyond 3 months in infants indicates need for intervention 1, 2
Repeat bone age: Annually if growth hormone is initiated 2
IGF-1 monitoring: At least twice yearly if on growth hormone therapy 5
Critical Pitfalls to Avoid
Initiating growth hormone before nutritional optimization: This is the most common error—nutrition is first-line therapy in infancy and can produce catch-up growth without hormonal intervention 1
Missing Turner syndrome: Always obtain karyotype in female infants with severe short stature, even without obvious dysmorphic features 2
Overlooking hypothyroidism: This completely reversible cause must be excluded before any growth hormone consideration 1
Ignoring metabolic acidosis: Uncorrected acidosis will prevent growth response to any intervention 1
Inadequate caloric delivery: Fluid restriction should never compromise caloric intake—use concentrated formulas or enteral feeding 1