Disease Comparison Results (show all mode) for Roussy-Levy syndrome and Reiger Syndrome

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Reiger Syndrome

Found: 51 | Differences: 47

Roussy-Levy syndrome

Found: 54 | Differences: 50

Roussy-Levy syndrome and Reiger Syndrome sharing 4 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms
Particular physiognomy/Odd looking kids
Broad flat nose/facies
Face broad/flat midface
Flat cheeks deformity/congenital
Midfacial hypoplasia/flat face dysmorphism
Prominent supraorbital ridges
Sunken Cheek Bones
Fetal Growth Rate Slowing
Everted umbilicus/prominent
Hypoplasia Narrow Maxilla
Large/protruding jaw/prognathism
Missing teeth/Aplastic
Small teeth/microdontia/pegs
Mental Deficiency Child
Finger contractions/flexion (clinodactyly)
Short fingers/toes (Brachydactyly)
Short stature
Short stature Child
Iris hypoplasia
Clinical Presentation & Variations
Presentation/Broad flat midface Nasal bridge Protruding jaw
Associated Diseases & Rule outs
Associated Disease & Complications
Axenfeld disease/iris
Congenital heart disease
Congenital/developmental dentition abnormalities
Dental deformities/anomalies
Eye Anomalies
Glaucoma
Mental retardation
Multiple Congenital Anomalies
Posterior Embryotoxon
Reiger Syndrome
Renal anomalies
Umbilibal Anomalies
Umbilical hernia
Disease Mechanism & Classification
Class
CLASS/Pediatric disorders (ex)
CLASS/Facial bones involvement/disorder (ex)
Pathophysiology
Pathophysiology/Gene locus 13q14
Pathophysiology/Gene locus 4q25-q27
Pathophysiology/Gene locus Chromosome 13
Pathophysiology/Gene locus chromosome 13q
Pathophysiology/Gene locus/Chromosome 4
Pathophysiology/Sporadic/hereditary/process
Pathophysiology/Gene mutation G551D
Pathophysiology/Gene mutation PITX2
Pathophysiology/Maternal Chromosome mutation
Process
PROCESS/Autosomal dominant hereditary disease (ex).
PROCESS/Congenital/developmental (category)
PROCESS/Eponymic (category)
PROCESS/Genetic disorder/Spontaneous mutations/sporadic
PROCESS/Hereditofamilial (category)
PROCESS/INCIDENCE/Rare disease (ex)
PROCESS/Anomalies/Deformities/Malformations (EX)
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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