Disease Comparison Results (show all mode) for Roussy-Levy syndrome and Severe combined immunodeficiency synd/SCID

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Severe combined immunodeficiency synd/SCID

Found: 151 | Differences: 139

Roussy-Levy syndrome

Found: 54 | Differences: 42

Roussy-Levy syndrome and Severe combined immunodeficiency synd/SCID sharing 12 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms
Buttock area rash
Rash
Acute Diarrhea
Acute Diarrhea in Children
Anorexia in Infant
Chronic Diarrhea in a Child
Diarrhea
Diarrhea in Children
Diarrhea, recurrent
Failure to Thrive
Failure to Thrive Child
Failure to thrive/infant sign
Feeding/Apetite Problems Child
Poor weight gain/child
Weight loss in Children
Absent tonsils/infant
Absent lymph nodes/infant
Cough
Cough Chronic
Recurrent chest infections/bronchitis/sign
Tonsil hypoplasia/absent
Fatigue Tiredness in Children
Fever, intermittant/recurrent
Growth/development delay
Sickly kid syndrome
Weight Loss
Clinical Presentation & Variations
Presentation/Recurrent Infections
Presentation/Lymphopenia Candidal diarrhea
Disease Progression
Course/Chronic disorder
Course/Chronic only
Course/Lethal
Course/Potentially lethal/untreated
Course/Prognosis bad/usually
Course/Recurrent
Course/Recurrent illness pattern
Lethal Potential
Onset/Six months
Demographics & Risk Factors
Population Group
Child
Infant
Population/Pediatrics population
Family History
Family history/Immune defects
Sex & Age Groups
Population/Child
Population/Child-Infant Only
Population/Children/all
Population/Infant
Population/Male
Laboratory Tests
Microbiology & Serology Findings
Common vaccination antibodies absent/low
Microlab/Mitogen lymphocyte response/vitro abnormal
Abnormal Lab Findings (Non Measured)
Chronic lymphopenia
DNATest specific/genetics laboratory/abnormality (Lab)
Lymphocyte low/absent CD3/Normal NK (CD16) (Lab)
Lymphocyte phenotype/panel abnormal (Lab)
Abnormal Lab Findings - Decreased
Circulating Total T-Cell Count
IGG/Immunoglobulin G (Lab)
IGM/Immunoglobulin M (Lab)
Lymphocytes (Lab)
Abnormal Lab Findings - Increased
Lymphocytes (Lab)
Diagnostic Test Results
Other Tests & Procedures
Skin test anergy
Skin test/DNCB (dinitrochlorobenzene) abnormal
Amniocentesis/Abnormality
Associated Diseases & Rule outs
Associated Disease & Complications - Rule Outs
Cystic fibrosis (mucoviscidosis)
Associated Disease & Complications - Causes
Agammaglobulinemia
Agammaglobulinemia, acquired
Anemia, aplastic
Anergic status
Cachexia/inanition/wasting
Candida albicans infection
Candidiasis, cutaneous
Cellular immunity defect/deficiency
Death Outcome
Diaper rash
Fungal/Candida endocarditis
Giardia infection/intestinal
Graft vs host reaction
Growth retardation/failure
Hypogammaglobulinemia
Hypogammaglobulinemia, acquired
Immunodeficiency
Infections
Intestinal/gut lymphoma
Lymphoblastic leukemia/acute
Lymphocytopenia
Lymphocytosis
Neonatal Erythroderma
Nodular lymphatoid hyperplasia/gut
Pneumococcus infection
Pneumocystis Jiroveci/Carinii Pneumonia (PCP)
Pneumonia, pneumococcal
Pneumonia, recurrent
Pneumonia, unresolved/Chronic
Pneumonia/Bronchopneumonia
Severe combined immunodeficiency syndrome
Staphylococcus aureus infection
Systemic mycosis/disseminated
Disease Mechanism & Classification
Class
CLASS/Humoral Immune System Disorder (ex)
CLASS/Immune System Disorder (ex)
CLASS/Pediatric disorders (ex)
CLASS/Spleen/thymus/RES/immune system (category)
Pathophysiology
Pathophysiology/Cytokine gene polymorphism
Pathophysiology/Fungal infection prone
Pathophysiology/Gene locus 11p13
Pathophysiology/Gene locus 13q14
Pathophysiology/Gene locus 16p13
Pathophysiology/Gene locus 19p12
Pathophysiology/Gene locus 1q21.1-q21.3
Pathophysiology/Gene locus Chromosome 1
Pathophysiology/Gene locus Chromosome 13
Pathophysiology/Gene locus Chromosome 16
Pathophysiology/Gene locus chromosome 19
Pathophysiology/Gene locus Chromosome X.
Pathophysiology/Gene Locus Identified/OMIM database
Pathophysiology/Gene locus Xq13
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Hereditary variance/ X-linked not always
Pathophysiology/Infection resistant to usual treatments
Pathophysiology/Absent Waldeyer ring/tonsils/nodes
Pathophysiology/Combined T-cell/B-cell immune deficiency
Pathophysiology/Decreased T Cells
Pathophysiology/Immune physiology/defective
Pathophysiology/Immune/cellular system disorder (ex)
Process
PROCESS/Disease with many subtypes (ex)
PROCESS/Hereditofamilial (category)
PROCESS/Heterogenous group of disorders (ex)
PROCESS/Sex-linked (X-linked) recessive inheritance (ex)
PROCESS/Variant expressions/Subsets (ex)
PROCESS/Immune system disorder (ex)
PROCESS/Immune/antibody-antigen system dis. (ex)
PROCESS/Immunodeficiency disorder/Primary
Synonyms
Synonym
Synonym/Agammaglobulinemia, Swiss type/SCID variant
Synonym/Autosomal recessive SCID syndrome/Variant
Synonym/Bare lymphocyte variant/SCID (19p12,16p13,13q14)
Synonym/Combined immunodeficiency syndrome/severe
Synonym/Lymphopenic agammaglobulinemia
Synonym/Reticular dysgenesis/SCID variant
Synonym/SCID syndrome
Synonym/SCID syndrome with lymphopenia/Variant
Synonym/SCID with reticuloendotheliosis (Ommens) variant
Synonym/T-cell kinase deficiency/SCID variant
Synonym/Thymic alymphoplasia/agammaglobulinemia
Synonym/Thymic dysplasia, hereditary
Synonym/X-linked progressive combined var. immunodef.
Synonym/X-linked recessive SCID syndrome
Treatment
Drug Therapy
RX/Gamma globulin/prophylaxis/low dose
RX/Pegademase (Adagen)
SX/Bone marrow transplant
SX/Stem cell transplant/allogenic
SX/Stem-cell transplant
Other Treatments
TX/Gene Therapy Possible
Clinical Manifestations
Signs & Symptoms
Absent knee reflexes
Ankle reflexes absent
Ankle reflexes decreased
Areflexia
Ataxia
Ataxia, Cerebellar type
Ataxia/Motor tremor type
Ataxia/Posterior columns
Babinski's upgoing toes/bilateral
Broad based/wide gait
Hyporeflexia/DTRs decreased
Neurologic manifestations/signs
Neurological symptoms/signs
Position sense decreased/proprioception
Position sense decreased/proprioception Legs
Sensory Ataxia
Staggering Gait
Unable to tandem walk/straight line
Unsteadiness movement/Gait in a child
Vibratory sense decreased
Weak reflexes
Disease Progression
Course/Chronic disorder
Course/Chronic only
Course/Normal life span/expectation
Course/Progressive/slowly chronic illness
Demographics & Risk Factors
Population Group
Child
Infant
Population/Pediatrics population
Family History
Family history/Nerve disease
Sex & Age Groups
Population/Child
Population/Child-Infant Only
Population/Children/all
Population/Infant
Associated Diseases & Rule outs
Associated Disease & Complications
Cerebellar ataxia
Pes cavus/High Arched Foot
Roussy-Levy syndrome
Spinal cord lesion/dysfunction
Ataxia Disorder
Disease Mechanism & Classification
Class
CLASS/Pediatric disorders (ex)
CLASS/Cerebellar disorder (ex)
CLASS/Neurologic (category)
CLASS/Spinal cord disorder (ex)
Pathophysiology
Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Pathophysiology/Developmental degeneration CNS
Pathophysiology/Posterior columns cord def
Process
PROCESS/Autosomal dominant hereditary disease (ex).
PROCESS/Eponymic (category)
PROCESS/Hereditofamilial (category)
PROCESS/INCIDENCE/Esoteric disease (example)
PROCESS/Use/Age/atrophic disorder (category)
PROCESS/Hereditary SCA (spinocerebellar ataxias)
Synonyms
Synonym
Synonym/Friedreichs/Roussy-Levy variant ataxia
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