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Differential Diagnosis For Xray/Air/gas in muscle/tendon/bursal areas, Muscles Soft/Doughy Infant


List of current finding(s):

Trauma Causes
Birth canal injury, newborn
Spinal cord injury
High cord injury
Fukuyama muscular dystrophy
Electromagnetic, Physics, trauma, Radiation Causes
Decompression sickness
Infectious Disorders (Specific Agent)
Newborn TORCH syndrome
Anaerobic bacterial infections
Gas gangrene
Post-viral/infectious encephalopathy
Poliomyelitis, paralytic, spinal
Myositis, bacterial, spontaneous
Infected organ, Abscesses
Acute infection
Newborn Sepsis Syndrome
Sepsis, overwhelming
Necrotizing fasciitis/mixed
Allergic, Collagen, Auto-Immune Disorders
Guillain-Barre syndrome
Isaacs potassium channel myopathy syndrome
Metabolic, Storage Disorders
Tay-Sachs disease
Combined carboxylase/Biotinidase deficiency
Cytochrome C Oxidase Deficiency/COX Complex Defect
French-Canadian type COX mitochondrial defect
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
Biochemical Disorders
Metabolic encephalopathy
Congenital, Developmental Disorders
Cerebral palsy
Down's Syndrome
Trisomy-21 partial translocation
Allan-Herndon Mental Retardation/X-linked
Shprintzen-Goldberg craniosynostosis syndrome (15q21.1)
Amyotonia, congenita
Hypotonia of Werdnig-Hoffman
Prader-Willi syndrome
Trisomy 13 syndrome
Birth asphyxia Syndrome/Hypoxic event
Central Hypotonia Infants
Coffin-Lowry Syndrome
Hereditary, Familial, Genetic Disorders
Hereditary neuropathy
Muscular dystrophy
Spinal muscle atrophy
Spinal muscle atrophy, infantile
Chromosome 22q13.3 deletion syndrome (22q13.3)
Juvenile spinal muscle atrophy (Kugelberg-Welander)
Mitochondrial myopathy/MERRF
Beckwith-Wiedemann Syndrome
MELAS Encephalopathy
Dominant SCA/Spinal Cerebellar ataxias
Borjeson-Forssman-Lehmann Syn/BFLS (xq26.3)
Canavan disease
Central core disease
Cerebellar ataxia, congenital/hered.
Dysautonomia, familial
Leukodystrophy, Krabbe
Muscular atrophy, infantile, spinal
Myotonia congenita (Thomsens d.)
Nemaline myopathy
Oculocerebrorenal dystrophy/Lowe syndrome
Progressive spinal muscular atrophy
Abducted thumbs syndrome
Congenital Muscular Dystrophy
Hereditary dysmyelinating neuropathy
Hereditary sensory neuropathy (type II)
Myopathy, Desmin Storage type/Sarcoplasmin bodies
Myopathy, Myotubular/Centronuclear
Say Syndrome 1
Welander syndrome (See Kugelberg Welander)
Anatomic, Foreign Body, Structural Disorders
Newborn intracranial hemorrhage
Spinal Cord Hematoma
Vegetative, Autonomic, Endocrine Disorders
Increased intracranial pressure
Myasthenia gravis
Neonatal myasthenia
Reference to Organ System
Spinal cord lesion
Hypotonia Syndrome Infant
Benzodiazepines Administration/Toxicity
Benzodiazepine toxicity/overdose
Poisoning (Specific Agent)
Botulism, infant
Organ Poisoning (Intoxication)
Toxic encephalopathy/poisoning