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Differential Diagnosis For Failure to Thrive Child: Hereditary, Familial, Genetic Disorders
- 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
- 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
Menkes steely hair disease
Oculocerebrorenal dystrophy/Lowe syndrome
Severe combined immunodeficiency synd/SCID
Williams syndrome/Elfin facies
Microvillous familial diarrhea/Davidson's synd
Ullrich Muscular Dystrophy