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Differential Diagnosis For Delay Sitting Unsupported Infant: Metabolic, Storage Disorders
List of current finding(s):
Delay Sitting Unsupported Infant
- Trauma Causes (5)
- Electromagnetic, Physics, trauma, Radiation Causes (1)
- Infectious Disorders (Specific Agent) (12)
- Infected organ, Abscesses (4)
- Allergic, Collagen, Auto-Immune Disorders (2)
- Metabolic, Storage Disorders (20)
- Biochemical Disorders (2)
- Congenital, Developmental Disorders (22)
- Hereditary, Familial, Genetic Disorders (33)
- Usage, Degenerative, Necrosis, Age Related Disorders (1)
- Anatomic, Foreign Body, Structural Disorders (2)
- Functional, Physiologic Variant Disorders (1)
- Vegetative, Autonomic, Endocrine Disorders (4)
- Reference to Organ System (2)
- Pathophysiologic (2)
- Drugs (3)
- Poisoning (Specific Agent) (8)
- Organ Poisoning (Intoxication) (2)
- Definition
- External Links Related to Delay Sitting Unsupported Infant
- Metabolic, Storage Disorders:
- Kernicterus
- Tay-Sachs disease
- Combined carboxylase/Biotinidase deficiency
- Cytochrome C Oxidase Deficiency/COX Complex Defect
- French-Canadian type COX mitochondrial defect
- Phenylketonuria/PKU
- Infantile mitochondrial myopathy/Cox defect
- Cerebral Gaucher's of infants (acute)
- Cerebral lipidosis disorder
- LCHAD/Long chain OH-CoA dehydrogenase def
- MCAD/Medium chain OH-CoA Dehydrogenase def
- VLCHAD/Very Long chain OH-CoA dehydrogenase def
- Carnitine deficiency syndrome
- Glutaric aciduria/type II
- Glycogen storage diseases
- Glycogen storage muscle disease/Pompe
- Mucolipidosis IV (Bermans Syndrome)
- Tetrahydrobiopterin deficiency/Atypical PKU
- Von Gierke's disease/glycogenosis I
- Lysosome Storage Disease
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