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Statements

Subject Item
dbr:Berdon_syndrome
rdf:type
yago:IllHealth114052046 yago:Content105809192 yago:WikicatAutosomalRecessiveDisorders yago:Idea105833840 yago:Concept105835747 yago:Complex105870365 yago:PathologicalState114051917 umbel-rc:AilmentCondition yago:Cognition100023271 yago:WikicatSyndromes yago:PsychologicalFeature100023100 dbo:Disease yago:GeneticDisease114151139 wikidata:Q12136 yago:State100024720 yago:Attribute100024264 yago:Syndrome105870790 yago:Whole105869584 yago:Disorder114052403 yago:Abstraction100002137 yago:PhysicalCondition114034177 owl:Thing yago:Condition113920835 yago:Illness114061805 yago:Disease114070360 yago:WikicatGeneticDisordersWithOMIMButNoGene
rdfs:label
متلازمة بيردون Megazystis-Mikrokolon-intestinale Hypoperistaltik-Syndrom Berdon syndrome
rdfs:comment
متلازمة بيردون (بالإنجليزية: Berdon syndrome)‏؛ وتعرف أيضا باسم متلازمة ، ، انكماش القولون،(بالإنجليزية: Megacystis-microcolon-intestinal hypoperistalsis syndrome)‏ وتختصر (MMIH)، تصيب الأطفال الرضّع والمواليد الجدد، وتكون سائدة أكثر عند الإناث. Das Megazystis-Mikrokolon-intestinale Hypoperistaltik-Syndrom (MMIHS) ist eine sehr seltene angeborene Erkrankung mit den namensgebenden Hauptmerkmalen zu große Harnblase (Megazystis), Mikrokolon, verminderte bis fehlende Peristaltik (Hypoperistaltik) des Darmes. S. 461 Das Syndrom wird von der Datenbank OMIM in Familiäre viszerale Myopathie eingegliedert. Synonym: Berdon-Syndrom Die Namensbezeichnung bezieht sich auf den Erstautor der Erstbeschreibung aus dem Jahre 1976 durch den US-amerikanischen Kinderradiologen W. E. Berdon und Mitarbeiter. Berdon syndrome, also called Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIH syndrome), is an autosomal recessive fatal genetic disorder affecting newborns. In a 2011 study of 227 children with the syndrome, "the oldest survivor [was] 24 years old." The Ann Arbor News reported a five year old survivor at the end of 2015.
foaf:name
Berdon syndrome
dbp:name
Berdon syndrome
foaf:depiction
n11:Autorecessive.svg
dcterms:subject
dbc:Genetic_disorders_with_OMIM_but_no_gene dbc:Syndromes_affecting_the_gastrointestinal_tract dbc:Syndromes_affecting_the_kidneys dbc:Autosomal_recessive_disorders
dbo:wikiPageID
1181346
dbo:wikiPageRevisionID
1017834559
dbo:wikiPageWikiLink
dbr:Urinary_bladder dbc:Autosomal_recessive_disorders dbr:Urinary_catheterisation dbr:Autosomal_recessive dbr:Inheritance dbr:Bowel dbr:Radiology dbr:Prune_belly_syndrome dbr:Recessive_gene dbr:Urinary_diversion dbr:Hydronephrosis dbr:Intestine dbr:Dominance_(genetics) dbr:Autosome dbr:The_Ann_Arbor_News dbc:Genetic_disorders_with_OMIM_but_no_gene dbr:Ganglion dbr:ACTG2 dbr:MYLK dbc:Syndromes_affecting_the_gastrointestinal_tract dbr:MYH11 dbc:Syndromes_affecting_the_kidneys dbr:Parenteral_nutrition dbr:Ileostomy dbr:Intestine_transplantation dbr:Megacystis dbr:LMOD1 dbr:Genetic_disorder dbr:Constipation dbr:Small_intestines dbr:Urinary_retention
owl:sameAs
dbpedia-ar:متلازمة_بيردون wikidata:Q4891136 freebase:m.04f2qk yago-res:Berdon_syndrome n21:4XzJf dbpedia-de:Megazystis-Mikrokolon-intestinale_Hypoperistaltik-Syndrom
dbp:wikiPageUsesTemplate
dbt:Reflist dbt:Citation_needed dbt:OMIM dbt:RareDiseases dbt:Infobox_medical_condition_(new) dbt:Medical_resources
dbo:thumbnail
n11:Autorecessive.svg?width=300
dbp:diseasesdb
32131
dbp:omim
249210
dbp:caption
Berdon syndrome has an autosomal recessive pattern of inheritance.
dbp:synonyms
Megacystis-microcolon-intestinal hypoperistalsis syndrome, MMIH syndrome, MMIHS
dbo:abstract
متلازمة بيردون (بالإنجليزية: Berdon syndrome)‏؛ وتعرف أيضا باسم متلازمة ، ، انكماش القولون،(بالإنجليزية: Megacystis-microcolon-intestinal hypoperistalsis syndrome)‏ وتختصر (MMIH)، تصيب الأطفال الرضّع والمواليد الجدد، وتكون سائدة أكثر عند الإناث. Das Megazystis-Mikrokolon-intestinale Hypoperistaltik-Syndrom (MMIHS) ist eine sehr seltene angeborene Erkrankung mit den namensgebenden Hauptmerkmalen zu große Harnblase (Megazystis), Mikrokolon, verminderte bis fehlende Peristaltik (Hypoperistaltik) des Darmes. S. 461 Das Syndrom wird von der Datenbank OMIM in Familiäre viszerale Myopathie eingegliedert. Synonym: Berdon-Syndrom Die Namensbezeichnung bezieht sich auf den Erstautor der Erstbeschreibung aus dem Jahre 1976 durch den US-amerikanischen Kinderradiologen W. E. Berdon und Mitarbeiter. Berdon syndrome, also called Megacystis-microcolon-intestinal hypoperistalsis syndrome (MMIH syndrome), is an autosomal recessive fatal genetic disorder affecting newborns. In a 2011 study of 227 children with the syndrome, "the oldest survivor [was] 24 years old." The Ann Arbor News reported a five year old survivor at the end of 2015. It is more prevalent in females (7 females to 3 males) and is characterized by constipation and urinary retention, microcolon, giant bladder (megacystis), intestinal hypoperistalsis, hydronephrosis and dilated small bowel. The pathological findings consist of an abundance of ganglion cells in both dilated and narrow areas of the intestine. It is a familial disturbance of unknown cause. Walter Berdon et al. in 1976 first described the condition in five female infants, two of whom were sisters. All had marked dilatation of the bladder and some had hydronephrosis and the external appearance of prune belly. The infants also had microcolon and dilated small intestines.
gold:hypernym
dbr:Disorder
prov:wasDerivedFrom
wikipedia-en:Berdon_syndrome?oldid=1017834559&ns=0
dbo:wikiPageLength
7361
dbo:diseasesDB
32131
dbo:omim
249210
foaf:isPrimaryTopicOf
wikipedia-en:Berdon_syndrome