Differential Diagnosis
Diseases
Drugs
More
[+] Tips
- Try building your search one term at a time, and be as specific as you can! Search term example: "chronic cough".
- Do not enter multiple findings such as "anemia, chronic cough, weight loss, vomiting" all at the same time.
- After selecting your term from the search results a list of possible diagnoses will be generated. If the list is too long, you will be able to narrow it down by entering additional terms.
- Do not enter values such as "heart rhythm 110" or "sodium 125", instead use "tachycardia" or "hyponatremia".

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

Clinical
Demographics
Diseases
Classification
Synonyms
Start Over

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

Ads

This site is designed primarily as a reminder system for use by qualified physicians and other medical professionals. By using this site you understand and accept that DiagnosisPro.com shall not be used as a diagnostic decision-making system and must not be used to make a clinical diagnosis or replace or overrule a licensed health care professional's judgment or clinical diagnosis (full terms of use). This site complies with the HONcode standard for trustworthy health information: verify here.