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- Disease Information
- Disease Comparison
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Disease Processes ▼
- Auto Immune
- Vascular-Arteriosclerosis
- Biochemical
- Congenital-developmental
- Deficiency
- Degenrative-Necrosis
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- Trauma
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Major Organs-Systems ▼
- Systemic
- Pediatric
- Nervous & Sensory System (Neurology)
- Cardiovascular System
- Respiratory (Pulmonary) System
- Gastro-Intestinal (Digestive) System
- Urinary System
- Dermatologic System
- Endocrine System
- Immune System
- Musculoskeletal System
- Genital Reproductive System
- Hematopoietic System (Hematology)
- Lymphatic System
- Tissue/Cells/Organelles
Disease Information for Cerebral Gaucher's of infants (acute)
- Clinical Manifestations
- Signs & Symptoms
- Hyperextensable Joints Infant
- Bruising/Ecchymosis
- Anorexia in Infant
- Failure to thrive/infant sign
- Feeding/Apetite Problems Child
- Tongue Protrudes Infant
- Hepatosplenomegaly
- Palpable Liver/Hepatomegaly
- Central hypotonia, infants
- Delay Sitting Unsupported Infant
- Hypotonia
- Mouth Hangs Open Infant
- Muscles Soft/Doughy Infant
- Rolling Over Delay Infant
- Babkin infant sign/Abnormal
- Central Facial Paralysis
- CNS symptoms/signs
- Delayed walking milestone/child
- Development Motor Skills (Milestones) Delayed
- Facial weakness/droop, unilateral
- Galant Infant reflex/Abnormal
- Head Neck Floppy Infant Hypotonia Sign
- Infant Head Support Delay
- Intellectual Decline Children
- Moro reflex Poor/Absent Infant
- Opisthotonus
- Palmar Grasp infant Reflex Abnormal
- Primitive infant reflexes/Abnormal
- Progressive neurological disorder/signs
- Rooting infant sign/Abnormal
- Stiff neck/Nuchal rigidity
- Swimming infant reflex/Abnormal
- Tonic Neck Infant reflex/Abnormal
- Shallow Breathing Infant
- Psychomotor retardation
- Bone Pains
- Delayed speech development/impediment
- Stridor (Inspiratory noise)
- Stridor infant Child
- Splenomegaly
- Cherry red spot/retinal sign
- Typical Clinical Presentation
- Presentation/Death in childhood
- Presentation/Progressive Neurologic disorder Infants
- Clinical Presentation & Variations
- Presentation/Acute encephalopathy Child
- Presentation/Degenerative cerebral disease Progressive Child
- Presentation/Mental Retardation Progressive
- Presentation/Opisthotonus Persistent Infant
- Disease Progression
- Course/Chronic disorder
- Course/Chronic only
- Demographics & Risk Factors
- Ethnic or Racial Factors
- Ashkenasi Jewish population
- Jewish population
- Established Disease Population
- Patient/Gauchers disease
- Population Group
- Child
- Infant
- Population/Pediatrics population
- Sex & Age Groups
- Population/Child
- Population/Child-Infant Only
- Population/Children/all
- Population/Infant
- Population/Young child ('Twos')
- Diagnostic Test Results
- Pathology
- PATH/Gliosis/Brain/CNS
- Associated Diseases & Rule outs
- Associated Disease & Complications
- Anemia
- Growth retardation/failure
- Infantile muscular spasms/Hypsarrhythmia
- Neonatal Hypotonia/Floppy Baby Syndrome
- Organomegaly
- Strabismus
- Thrombocytopenia
- Disease Mechanism & Classification
- Class
- CLASS/Pediatric disorders (ex)
- CLASS/Brain/CNS disorder (ex)
- CLASS/Neurologic (category)
- Pathophysiology
- Pathophysiology/Gene locus Chromosome 1
- Pathophysiology/Lysosome storage disorder (ex)
- Pathophysiology/Congenital Brain malformation
- Pathophysiology/Ganglioside accumulation brain
- Pathophysiology/84insG Gene mutation
- Pathophysiology/Beta Glucosidase Defect
- Pathophysiology/Gene locus 1q21-q31
- Pathophysiology/Glucosylceramide accumulates
- Pathophysiology/IVS2 Gene mutation
- Pathophysiology/L444P Gene mutation
- Pathophysiology/N370S gene mutation
- Process
- PROCESS/Autosomal recessive disorder (ex)
- PROCESS/Metabolic/storage disorder (category)
- PROCESS/Storage disorder (ex)
- PROCESS/Cerebral lipidoses (ex)
- PROCESS/Congenital CNS disorder (ex)
- PROCESS/Storage disorder/brain (ex)
- Synonyms
- Synonym
- 0 11 years old, ACID BETA GLUCOSIDASE DEFIC DIS, ACID BETA GLUCOSIDASE DEFICIENCY, Acid beta Glucosidase Deficiency Disease, acute, Adult Gaucher disease, ANEMIA SPLENIC FAMILIAL, cerebroside lipidosis, Cerebroside lipidosis syndrome, CEREBROSIDE LIPOIDOSIS (GAUCHERS ADULT FORM), CEREBROSIDE LIPOIDOSIS GAUCHERS ADULT FORM, Child, Child (person), Child Youth, Childhood age person, Childhood age person (person), Children, Children (0 21), Chronic adult Gaucher's disease, CHRONIC GAUCHER DIS, Chronic Gaucher Disease, Chronic non neuropathic Gaucher's disease, Chronic non neuropathic Gaucher's disease (disorder), familial splenic anemia, GAUCHER DIS, GAUCHER DIS CHRONIC, GAUCHER DIS NON NEURONOPATHIC FORM, GAUCHER DIS TYPE I, Gaucher disease, Gaucher Disease Chronic, Gaucher Disease Non Neuronopathic, Gaucher Disease Non Neuronopathic Form, GAUCHER DISEASE NONCEREBRAL JUVENILE, Gaucher Disease Type 1, GAUCHER DISEASE TYPE I, Gaucher splenomegaly, Gaucher syndrome, GAUCHERS DIS, Gauchers Disease, Gaucher's disease, Gaucher's disease type I, GBA DEFICIENCY, GD I, Glucocerebrosidase def type I, GLUCOCEREBROSIDASE DEFIC DIS, Glucocerebrosidase deficiency, Glucocerebrosidase Deficiency Disease, Glucocerebrosidase Deficiency Diseases, Glucocerebrosidase deficiency type I, Glucocerebrosidosis, GLUCOSYL CEREBROSIDE LIPIDOSIS, Glucosylceram b glucosidas def, glucosylceramidase deficiency, Glucosylceramidase deficiency chronic type, GLUCOSYLCERAMIDE BETA GLUCOSIDASE DEFIC DIS, Glucosylceramide beta glucosidase deficiency, Glucosylceramide beta glucosidase deficiency (disorder), Glucosylceramide Beta Glucosidase Deficiency Disease, glucosylceramide lipidosis, HISTIOCYTOSIS LIPID KERASIN TYPE, Kerasin histiocytosis, Kerasin lipoidosis, Kerasin thesaurismosis, Kerasin thesaurismosis (disorder), lipidosis cerebroside, lipoid histiocytosis (kerasin type), NON NEURONOPATHIC GAUCHER DIS, Non Neuronopathic Gaucher Disease, splenomegaly gaucher's, TYPE 1 GAUCHER DIS, Type 1 Gaucher Disease, Synonym/Gauchers Disease/Type II
- Treatment
- Drug Therapy - Indication
- RX/Imiglucerase (Cerezyme)
- SX/Bone marrow transplant
- Definition
- Be the first to add a definition for Cerebral Gaucher's of infants (acute)
- External Links Related to Cerebral Gaucher's of infants (acute)
- 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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