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Differential Diagnosis For Failure to Thrive Child: Congenital, Developmental Disorders
List of current finding(s):
Failure to Thrive Child
- Trauma Causes (2)
- Electromagnetic, Physics, trauma, Radiation Causes (1)
- Infectious Disorders (Specific Agent) (16)
- Infected organ, Abscesses (6)
- Granulomatous, Inflammatory Disorders (1)
- Neoplastic Disorders (2)
- Allergic, Collagen, Auto-Immune Disorders (7)
- Metabolic, Storage Disorders (29)
- Deficiency Disorders (8)
- Congenital, Developmental Disorders (47)
- Hereditary, Familial, Genetic Disorders (14)
- Relational, Mental, Psychiatric Disorders (2)
- Anatomic, Foreign Body, Structural Disorders (4)
- Arteriosclerotic, Vascular, Venous Disorders (1)
- Functional, Physiologic Variant Disorders (9)
- Vegetative, Autonomic, Endocrine Disorders (14)
- Reference to Organ System (10)
- Pathophysiologic (2)
- Heirarchical Major Groups (1)
- Drugs (1)
- Poisoning (Specific Agent) (6)
- Definition
- External Links Related to Failure to Thrive Child
- Congenital, Developmental Disorders:
- Hyaline membrane/immature lung newborn
- Congenital disorders
- Cleft lip
- Down's Syndrome
- 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
- Placenta insufficiency syndrome/infant
- 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 goiter
- 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)
- Hypotonia of Werdnig-Hoffman
- Laron dwarfism/GH receptor defect
- Lung dysplasia/hypoplasia/infant
- Pierre Robin syndrome
- Prader-Willi syndrome
- Silver-Russell syndrome
- Trisomy 13 syndrome
- Trisomy-18 syndrome
- Bowen Conradi/Bowen Hutterite Syndrome
- Congenital Central Lymphatics Obstruction/Dysplasia
- Vein of Galen/AVM congenital
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