About: Berdon syndrome

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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.

Attributes	Values
rdf:type	Thing Disease yago:WikicatAutosomalRecessiveDisorders yago:Abstraction100002137 yago:Attribute100024264 yago:Cognition100023271 yago:Complex105870365 yago:Concept105835747 yago:Condition113920835 yago:Content105809192 yago:Disease114070360 yago:Disorder114052403 yago:GeneticDisease114151139 yago:Idea105833840 yago:IllHealth114052046 yago:Illness114061805 yago:PathologicalState114051917 yago:PhysicalCondition114034177 yago:PsychologicalFeature100023100 yago:WikicatGeneticDisordersWithOMIMButNoGene disease yago:State100024720 yago:Syndrome105870790 yago:Whole105869584 yago:WikicatSyndromes umbel-rc:AilmentCondition
rdfs:label	Berdon syndrome (en) متلازمة بيردون (ar) Megazystis-Mikrokolon-intestinale Hypoperistaltik-Syndrom (de)
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. (ar) 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. (de) 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. (en)
foaf:name	Berdon syndrome (en)
name	Berdon syndrome (en)
foaf:depiction
dcterms:subject	Autosomal recessive disorders Syndromes affecting the gastrointestinal tract Syndromes affecting the kidneys Genetic disorders with OMIM but no gene
Wikipage page ID	1181346 (xsd:integer)
Wikipage revision ID	1017834559 (xsd:integer)
Link from a Wikipage to another Wikipage	Prune belly syndrome MYLK The Ann Arbor News Urinary bladder Urinary catheterisation Inheritance Genetic disorder Constipation Autosomal recessive disorders MYH11 Parenteral nutrition Autosomal recessive Ganglion Syndromes affecting the gastrointestinal tract Syndromes affecting the kidneys Urinary retention Intestine transplantation Hydronephrosis ACTG2 Genetic disorders with OMIM but no gene Small intestines Dominance (genetics) Autosome Ileostomy Recessive gene Radiology Urinary diversion Intestine Megacystis Bowel dbr:LMOD1
sameAs	Berdon syndrome Berdon syndrome Berdon syndrome Berdon syndrome Berdon syndrome Berdon syndrome
dbp:wikiPageUsesTemplate	dbt:Citation_needed dbt:Infobox_medical_condition_(new) dbt:Medical_resources dbt:Reflist dbt:OMIM dbt:RareDiseases
thumbnail	wiki-commons:Special:FilePath/Autorecessive.svg?width=300
DiseasesDB	32131 (xsd:integer)
OMIM	249210 (xsd:integer)
caption	Berdon syndrome has an autosomal recessive pattern of inheritance. (en)
synonyms	Megacystis-microcolon-intestinal hypoperistalsis syndrome, MMIH syndrome, MMIHS (en)
has 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. (ar) 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. (de) 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. (en)
gold:hypernym	Disorder
prov:wasDerivedFrom	wikipedia-en:Berdon_syndrome?oldid=1017834559&ns=0
page length (characters) of wiki page	7361 (xsd:nonNegativeInteger)
DiseasesDB	32131
OMIM id	249210 (xsd:integer)
foaf:isPrimaryTopicOf	wikipedia-en:Berdon_syndrome
is Link from a Wikipage to another Wikipage of	List of diseases (B) List of eponymous diseases

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