- Home
- |
- What is DiagnosisPro?
- |
- Contact Us
- |
- Sign In
- |
- More
- |
Differential Diagnosis for Failure to thrive/infant sign
defective thrive, Failure to thrive, Failure to thrive (disorder), Failure to thrive syndrome, Failure-to-thrive, FTT Failure to thrive, Infant, thrive failure, Thrive Failure to (less)
defective thrive, Failure to thrive, Failure to thrive (disorder), Failure ... (more)
162 possible diagnoses found. Too many? Narrow results
Trauma Causes
Infectious Disorders (Specific Agent)
- Newborn TORCH syndrome
- Neonatal chlamydial pneumonia
- Neonatal pneumonia, bacterial
- Herpes simplex infection, newborn, gen
- Immune deficiency , acquired (AIDS/HIV)
- Intestinal parasites
- Neonatal hepatitis
- AIDS Wasting Syndrome
- Tuberculosis
- Listeria hepatitis, newborn
- Rubella hepatitis, newborn
- Cytomegalic virus, congenital
- Syphilis, congenital
- Toxoplasmosis, congental
- Tracheobronchial tuberculosis
- Tuberculosis pulmonary
Infected organ, Abscesses
Granulomatous, Inflammatory Disorders
Neoplastic Disorders
Allergic, Collagen, Auto-Immune Disorders
Metabolic, Storage Disorders
- Diabetes mellitus
- Renal tubular disorders/metabolic
- Diabetes mellitus/juvenile (Type I)
- Kernicterus
- Renal tubular acidosis type IV
- Xanthinuria
- Newborn diabetes mellitus, transient
- Methylmalonic acidemia/ketotic glycine
- Acyl-CoA Dehydrogenase/short chain def
- Aminoacid enzyme/metabolic disorder
- Cerebral Gaucher's of infants (acute)
- LCHAD/Long chain OH-CoA dehydrogenase def
- MCAD/Medium chain OH-CoA Dehydrogenase def
- Tyrosinemia, hereditary
- VLCHAD/Very Long chain OH-CoA dehydrogenase def
- Aminoaciduria
- Carnitine deficiency syndrome
- Farber disease/ceramide lipidosis
- Fructose intolerance, hereditary
- Fucosidosis (Anderson-Fabry)
- Galactosemia
- Gangliosidosis, generalized (GM1)
- Glycogen storage diseases
- Maple syrup urine disease
- Niemann-Pick disease
- Phosphoenolpyruvate carboxykinase defic (PEPCK)
- Storage (storage-cell) disorders
Deficiency Disorders
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 heart disease
- Placenta insufficiency syndrome/infant
- Plethora of newborn
- Renal tubular acidosis
- Renal tubular acidosis, proximal/type 2
- Atrioventricular canal/cushion defect
- Congenital renal/urological anomalies
- Distal renal tubular acidosis/type 1
- Neonatal goiter
- Neonatal Graves/thyrotoxicosis disease
- Thymus hypoplasia/DiGeorge syndrome
- Trisomy-21 partial translocation
- Turner's syndrome/Gonadal dysgenesis
- Jejunal Atresia congenital syndrome (unco)
- Duodenum, atresia
- Esophagus, atresia
- Pyloric stenosis ,congenital
- 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
Hereditary, Familial, Genetic Disorders
- Agammaglobulinemia, x-linked, infantile
- Cystic fibrosis (mucoviscidosis)
- Johanson Blizzard genetic syndrome (unco)
- Wiskott-Aldrich syndrome
- Acrodermatitis enteropathica
- Borjeson-Forssman-Lehmann Syn/BFLS (xq26.3)
- Cockayne syndrome
- Encephalomyelopathy/necro/subact/Leigh
- Oculocerebrorenal dystrophy/Lowe synd
- Severe combined immunodeficiency synd/SCID
- Williams syndrome/Elfin facies
Relational, Mental, Psychiatric Disorders
Anatomic, Foreign Body, Structural Disorders
Arteriosclerotic, Vascular, Venous Disorders
Functional, Physiologic Variant Disorders
Vegetative, Autonomic, Endocrine Disorders
- Esophageal free reflux/GERD syndrome
- Hyperthyroid status
- Thyrotoxicosis (Graves disease)
- Hypothyroidism (myxedema)
- Diabetes insipidus
- Pituitary hypothyroidism
- Primary hypothyroidism/myxedema
- Dwarfism, panhypopituitary
- Growth hormone deficiency
- Hypothyroidism, juvenile
- Panhypopituitarism
- Byler/intrahepatic cholestasis syndrome
- Diencephalic syndrome
- Esophageal reflux/infant rumination
Reference to Organ System
Pathophysiologic
Heirarchical Major Groups
Poisoning (Specific Agent)
External Links Related to Failure to thrive/infant sign
Navigation
Start a New Case
Suggest a Missing Condition/Disease
What is DiagnosisPro?
DiagnosisPro is a free, accurate and time saving differential diagnosis tool that reminds you instantly of diagnostic possibilities and minimizes medical errors.
Overview
- Covering over 15,000 disease manifestations such as symptoms, labs, ECG, X-ray, CT-Scan, MRI, Ultrasound, pathology, microbiology results and more.
- Compiled from hundreds of world's most respected medical resources covering internal medicine, emergency medicine, pediatrics, office OB-GYN and more.
- Designed for physicians by physicians to enhance quality of care and prevent diagnostic errors.
- Detailed disease information for more than 7000 diseases.
- Disease comparison tool to compare any two diseases side by side.
Join Our Community
Suggest improvement to our data or add your interesting cases to share with tens of thousands of other physicians worldwide.
This site is designed primarily as a reminder system for use by qualified physicians and other medical professionals. By using this site you understand and accept that DiagnosisPro.com shall not be used as a diagnostic decision-making system and must not be used to make a clinical diagnosis or replace or overrule a licensed health care professional's judgment or clinical diagnosis (full terms of use).
© 2009 MedTech USA, Inc. (last modified on 01/09/09)