Disease Information for Cerebral Gaucher's of infants (acute)
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
(less)
0 11 years old, ACID BETA GLUCOSIDASE DEFIC DIS, ACID BETA GLUCOSIDASE DEFI... (more)
[Add a definition for Cerebral Gaucher's of infants (acute)]
64 related Findings found. Compare "Cerebral Gaucher's of infants (acute)" to ...?
Demographics & Risk Factors[next]
- Established Disease Population
- Population Group
- Population/Pediatrics population
- Sex & Age Groups
- Population/Child
- Population/Child-Infant Only
- Population/Children/all
- Population/Infant
- Population/Young child ('Twos')
Clinical Manifestations[previous][top][next]
- Typical Clinical Presentation
- Presentation/Acute encephalopathy/child
- Presentation/Death in childhood
- Presentation/Degenerative cerebral dis/progressive/child
- Presentation/Mental retardation progressive
- Presentation/Opisthotonus/persistant/infant
- Presentation/Progressive neurologic dis/infants
- Disease Progression
- Course/Chronic disorder
- Course/Chronic only
- Signs & Symptoms
- Child
- Infant
- Bruising/Ecchymosis
- Failure to thrive/infant sign
- Hepatomegaly
- Hepatosplenomegaly
- Central hypotonia, infants
- Hypotonia
- Central Facial Paralysis
- CNS symptoms/signs
- Facial weakness/droop, unilateral
- Neonatal hypotonia/floppy-baby sign
- Opisthotonus
- Progressive neurological disorder/signs
- Stiff neck/Nuchal rigidity
- Psychomotor retardation
- Bone Pain
- Delayed speech development/impediment
- Stridor
- Splenomegaly
- Typical Clinical Presentation
Diagnostic Test Results[previous][top][next]
- Pathology
Associated Diseases & Rule outs[previous][top][next]
- Associated Disease & Complications
Disease Mechanism & Classification[previous][top][next]
- 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
- Pathophysiology/Organomegaly
- Process
- PROCESS/Metabolic/storage disorder (category)
- PROCESS/Storage disorder (ex)
- PROCESS/Cerebral lipidoses (ex)
- PROCESS/Congenital CNS disorder (ex)
- PROCESS/Storage disorder/brain (ex)
- Class
-
- Synonym
- Synonym/Gauchers Disease/Type II
- Synonym
Treatment[previous][top][next]
- Drug Therapy - Indication
- RX/Imiglucerase (Cerezyme)
- SX/Bone marrow transplant
- Drug Therapy - Indication
External Links Related to Cerebral Gaucher's of infants (acute)[previous][top]
What is DiagnosisPro?
DiagnosisPro is a free, accurate and time saving differential diagnosis tool that reminds you instantly of diagnostic possibilities and minimizes medical errors.
Overview
- Covering over 15,000 disease manifestations such as symptoms, labs, ECG, X-ray, CT-Scan, MRI, Ultrasound, pathology, microbiology results and more.
- Compiled from hundreds of world's most respected medical resources covering internal medicine, emergency medicine, pediatrics, office OB-GYN and more.
- Designed for physicians by physicians to enhance quality of care and prevent diagnostic errors.
- Detailed disease information for more than 7000 diseases.
- Disease comparison tool to compare any two diseases side by side.
Join Our Community
Suggest improvement to our data or add your interesting cases to share with tens of thousands of other physicians worldwide.

