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Disease Comparison Results (show all mode) for Meckel-Gruber syndrome and Weill-Marchesani syndrome

Clinical
Demographics
Diagnostic
Diseases
Classification
Synonyms
Treatment
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Found: 28 | Differences: 18

Found: 59 | Differences: 49

Meckel-Gruber syndrome and Weill-Marchesani syndrome sharing 10 common findings. (show all, show common, show differences)

Clinical Manifestations
Signs & Symptoms: Dysmorphic dwarfism/short stature; Dysmorphic appearance/face; Short stature; Short stature Child; Eye symptoms/signs; Small lens/congenital/sign
Disease Progression: Course/Chronic disorder; Course/Chronic only

Demographics & Risk Factors
Population Group: Child; Population/Pediatrics population
Family History: Family history/Dwarfism
Sex & Age Groups: Population/Child; Population/Child-Infant Only; Population/Children/all

Associated Diseases & Rule outs
Associated Disease & Complications: Congenital heart disease; Dwarfism; Nanism/dwarfism; Patent ductus arteriosis

Disease Mechanism & Classification
Class: CLASS/Ophthalmology Specialty Population; CLASS/Pediatric disorders (ex); CLASS/Skeletal (category); CLASS/Ophthalmology disorders; CLASS/Eye involvement/disorder (ex); CLASS/Eyes/accessory (category)
Pathophysiology: Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations)
Process: PROCESS/Eponymic (category); PROCESS/Hereditofamilial (category); PROCESS/Multiple dysmorphic syndrome (ex)

Clinical Manifestations
Signs & Symptoms: Flat/Sloping forehead; Uvula anomaly/deformity; Bowing of extremities; Foot deformity; Sudden death of an infant; Narrow Palpebral Fissures
Clinical Presentation & Variations: Presentation/Kidney malformations Congenital syndrome Child
Disease Progression: Course/Chronic only; Course/Lethal

Demographics & Risk Factors
Ethnic or Racial Factors: Arab/population; Finnish population
Population Group: Child; Population/Pediatrics population
Sex & Age Groups: Population/Child; Population/Child-Infant Only; Population/Children/all

Diagnostic Test Results
Pathology: PATH/Occipital encephalocele/fetus

Associated Diseases & Rule outs
Associated Disease & Complications: Cataract; Cleft Lip; Cleft lip/deformity; Cleft palate/deformity; Clubbed foot/congenital; Congenital anomalies; Death Newborn/Perinatal; Genital anomalies/caused; Infantile Polycystic kidney disease; Limb deformities/anomalies; Meckel-Gruber syndrome; Meningoencephalocele; Microcephaly/oligophrenia; Microphthalmos; Polycystic kidney disease; Polydactyly/Supernumery digits; Recurrent GI Bleeding; Renal cyst; Stillborn; Sudden death/Child; Hand anomalies

Disease Mechanism & Classification
Class: CLASS/Pediatric disorders (ex); CLASS/Fetal/conceptual products (category); CLASS/Intestinal/stomach/gut (category)
Pathophysiology: Pathophysiology/Gene locus chromosome 12; Pathophysiology/Gene locus chromosome 12q; Pathophysiology/Gene locus Chromosome 17q; Pathophysiology/Gene locus Chromosome 8q; Pathophysiology/Genomic indentifiers (polymorphism/snip/mutations); Pathophysiology/MKS1 Gene Mutation; Pathophysiology/MKS2 Gene Mutation; Pathophysiology/Gene locus chromosome 8
Process: PROCESS/Autosomal recessive disorder (ex); PROCESS/Congenital/developmental (category); PROCESS/Eponymic (category); PROCESS/Hereditofamilial (category); PROCESS/INCIDENCE/Esoteric disease (example); PROCESS/Anomalies/Deformities/Malformations (EX); PROCESS/Lethal perinatal/Incompatible with survival

Synonyms
Synonym: Synonym/Dysencephalia splanchnocystica; Synonym/Meckel syndrome

Treatment
Other Treatments: TX/Genetic counselling

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