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Possible Causes For Growth retardation/failure - Causes
List of current finding(s):
Growth retardation/failure - Causes
- Infected organ, Abscesses
- Osteomyelitis, pyogenic chronic
- Neoplastic Disorders
- Craniopharyngioma
- Allergic, Collagen, Auto-Immune Disorders
- Juvenile rheumatoid arthritis/Stills d
- Juvenile chronic arthritis (rheumatoid)
- Metabolic, Storage Disorders
- Neonatal hyperbilirubinemia
- Hurler's mucopolysaccharidosis syndrome
- Cerebral Gaucher's of infants (acute)
- Valinemia/Hypervalinemia
- Fructose intolerance, hereditary
- Fucosidosis (Anderson-Fabry)
- Galactosemia
- Gangliosidosis, generalized (GM1)
- Glycogen storage diseases
- Hepatophosphorylase def. glycogenosis
- Histidinemia
- Lesch-Nyhan syndrome
- Phosphoenolpyruvate carboxykinase defic (PEPCK)
- Von Gierke's disease/glycogenosis I
- Barth Syndrome/3 MethylGlutoconic aciduria/MGA II
- Deficiency Disorders
- Iron deficiency anemia
- Malnutrition/Starvation
- Avitaminosis A
- Hypovitaminosis A
- Zinc deficiency
- Congenital, Developmental Disorders
- Medullary cystic kidney disease
- Growth/Developmental disorders
- Atrioventricular canal/cushion defect
- Cretinism
- Cri du Chat/Chromosome 5p (5p15.2)
- Multiple lentigenes syndrome (congenit)
- Alexander disease
- Mulibrey Nanism syndrome
- Alagille/Arteriohepatic dysplasia syndr
- Bloom syndrome
- Chromosome 4p-syndrome
- De Lange syndrome
- Dubowitz syndrome
- Hallermann-Streiff-Francois syndrome
- Noonan syndrome
- Progeria
- Progeria of child (Hutchinson-Gilford)
- Rett's syndrome
- Shawl scrotum syndrome
- Trichorhinophalangeal congenital synd
- Velocardiofacial (22q gene) syndrome
- Carpenter Syndrome
- CODAS Syndrome
- Porteous Syndrome
- Primary protein losing enteropathy syndrome
- Ruvacaba's Syndrome
- Hereditary, Familial, Genetic Disorders
- Granulomatous dis/childhood, chronic
- Thalassemia major
- Sickle cell anemia
- Ataxia-telangiectasia
- Cleidocranial digital dysostosis
- Cystic fibrosis (mucoviscidosis)
- Nephritis, hereditary (Alports)
- Osteogenesis imperfecta
- Fechtner syndrome/FTNS (22q11.2)
- Johanson Blizzard genetic syndrome (unco)
- Juberg Marsidi Genetic syndrome (unco)
- Myhre Syndrome
- Neonatal Progeria Familial (Wiedemann)
- Pitt syndrome (4p16.3)
- Acrodermatitis enteropathica
- Bartter's syndrome
- Bird-headed dwarf of Seckel
- Hyperphosphatasia, hereditary
- Menkes steely hair disease
- Scott's Craniodigital syndrome
- Severe combined immunodeficiency synd/SCID
- Smith-Lemli-Opitz syndrome
- Spondylometaphyseal dysplasia syndrome
- Williams syndrome/Elfin facies
- Brooks syndrome
- Hereditary Transferrin deficiency/Aferritinemia
- Kabuki make-up syndrome
- Vegetative, Autonomic, Endocrine Disorders
- Hypothyroidism (myxedema)
- Pituitary hypofunction, anterior
- Cushing's disease/Syndrome
- Hypothyroidism, juvenile
- Panhypopituitarism
- Reference to Organ System
- Growth impairment
- Renal osteodystrophy
- Protein losing enteropathy
- Hypogammaglobulinemia/Agammaglobulinemia
- Heirarchical Major Groups
- Pancreas disorders
- Drugs
- Anabolic steroid hormone Administration/Toxicity
- Hypervitaminosis D
- Accutane (ITR) embryopathy syndrome
- Poisoning (Specific Agent)
- Fetal alcohol syndrome
- Synonyms
- Decreased growth, Growth retardation, Growth retardation (morphologic abnormality), Growth retarded, Growth suppression, Retardation, retardation growth, Retarded growth
- Definition
- Be the first to add a definition for Growth retardation/failure - Causes
- External Links Related to Growth retardation/failure - Causes
- Wikipedia
- Merck
- Images
- PubMed (National Library of Medicine)
- NGC (National Guideline Clearinghouse)
- Medscape (eMedicine)
- Harrison's Online (accessmedicine)
- NEJM (The New England Journal of Medicine)
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