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Differential Diagnosis For Failure to Thrive: Congenital, Developmental Disorders

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Failure to Thrive
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Congenital, Developmental Disorders: next: Genetic Causes: Hyaline membrane/immature lung newborn; Congenital disorders; Down's Syndrome; Hemorrhagic disease of newborn; Pyloric stenosis, cong. hypertrophic; Cleft palate/palate incompetence; Congenital acyanotic heart disease; Congenital CNS Ventricular outflow dfct; Congenital cyanotic heart disease; Congenital heart disease; Cretinism, goitrous sporadic; Plethora of newborn; Renal tubular acidosis; Renal tubular acidosis, proximal/type 2; Atrioventricular canal/cushion defect; Congenital renal/urological anomalies; Cretinism; Distal renal tubular acidosis/type 1; Lung hypoplasia/congenital/child; Neonatal Graves/thyrotoxicosis disease; Thymic aplasia, congenital (DiGeorges); Thymus hypoplasia/DiGeorge syndrome; Trisomy-21 partial translocation; Turner syndrome/Gonadal dysgenesis; Jejunal Atresia congenital syndrome (unco); Duodenum, atresia; Esophagus, atresia; Tracheoesophageal fistula; Bile duct atresia; Intestine malrotation; Shunt, intracardiac; Agammaglobulinemia, congenital/autosomal; Anomalous origin innominate artery; Craniocarpotarsal Dystrophy (Freeman Sheldon); Lung dysplasia/hypoplasia/infant; Pierre Robin syndrome; Prader-Willi syndrome; Silver-Russell syndrome; Trisomy 13 syndrome; Trisomy-18 syndrome; Turner mosaic syndrome; Bowen Conradi/Bowen Hutterite Syndrome; Congenital Central Lymphatics Obstruction/Dysplasia; Vein of Galen/AVM congenital

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