Patent urachus

Patent urachus is a type of congenital urachal anomaly (see this term) characterized by a persistent communication between the bladder and the umbilicus, secondary to non occlusion of the urachal lumen, manifesting as clear drainage from the umbilicus.



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Total: 51 (papers)

  


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Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(63.7%)
9856555
Blepharophimosis, hypoplastic radius, hypoplastic left heart, telecanthus, hydronephrosis, fused metacarpals, and "prehensile" halluces: a new syndrome?
Day-Salvatore D, McLean D.
Am J Med Genet. 1998;80(4):309-13.
Micrognathia Telecanthus Tibial bowing
Adult Blepharophimosis Congenital Foot Deformity Congenital Hand Deformities Congenital Heart Defects Differential Diagnosis Eye Abnormalities Females Homo sapiens Hydronephrosis Infant Infant, Newborn Pregnancy Syndrome
2
(45.9%)
20204225
[Gollop-Wolfgang complex and cloacal exstrophy, a strange association].
Cruz-Pareja E, Garcia-Santibanez R, Jaramillo Sotomayor C, Carriel Mancilla J, Lopez Moncayo J, Jurado Flores M, Landivar Varas X.
Arch Argent Pediatr. 2010;108(1):e1-4.
Metabolic acidosis Absent tibia
Fatal Outcome Femur Homo sapiens Infant, Newborn Toes
3
(21.2%)
12685093
Patent urachus with subsequent joint infection in a free-living Grevy's zebra foal.
Ndung'u FK, Ndegwa MW, deMaar TW.
J Wildl Dis. 2003;39(1):244-5.
Arthritis
Animals Animals, Newborn Animals, Wild Arthritis, Infectious Bacteremia Equidae Escherichia coli Escherichia coli Infections Fatal Outcome Females Urachus
4
(17.5%)
26667556
MANAGEMENT OF OMPHALOPHLEBITIS AND UMBILICAL HERNIA IN THREE NEONATAL GIRAFFE (GIRAFFA CAMELOPARDALIS).
Selig M, Lewandowski A, Burton MS, Ball RL.
J Zoo Wildl Med. 2015;46(4):938-40.
Umbilical hernia
Animals Animals, Newborn Male Peritonitis Phlebitis
5
(4.0%)
31139338
Acute abdomen due to an infected urachal cyst in a 5-year-old female: case report.
Kudra Danial A, Sankari Tarabishi A, Aldakhil A, Alzahran A, Najjar O, Ayoub K.
J Surg Case Rep. 2019;2019(5):rjz156.
Fever
5
(4.0%)
31037039
Infection of Previously Closed Urachus Mimicking Malignancy: A Case Report and Literature Review of Radiological Findings to the Diagnosis.
Lam SW, Linsen PV, Elgersma OE.
Clin Med Insights Case Rep. 2019;12:1179547619843836.
Abdominal mass
5
(4.0%)
30671379
Enterourachal Fistula as an Initial Presentation in Crohn Disease.
Sankararaman S, Sabe R, Sferra TJ, Khalili AS.
Pediatr Gastroenterol Hepatol Nutr. 2019;22(1):90-97.
Abdominal pain
5
(4.0%)
29650846
[Two-Stage Radical Resection of a Case of Colon Cancer with Abdominal Wall Invasion and Cholangiocarcinoma].
Sugimoto T, Kiyochi H, Hosoda Y, Komoto I, Sasaki Y, Nishiyama K, Katayama H, Ogura N, Tsunekawa S, Taki Y, Akahane M, Aoyama T, Matsumoto H, Takami S, Kawai J.
Gan To Kagaku Ryoho. 2018;45(4):718-720.
Fever
Bile Duct Neoplasms Cholangiocarcinoma Colonic Neoplasms Females Homo sapiens Middle Aged Neoplasm Invasiveness Neoplasms, Multiple Primary
5
(4.0%)
29318419
Prolapsed bladder following rupture of patent urachal cyst, mimicking bladder exstrophy: a case report and literature review.
Srisupundit K, Mahawong P, Charoenratana C, Tongsong T.
J Med Ultrason (2001). 2018;45(3):529-533.
Epispadias
Adult Differential Diagnosis Females Fetal Diseases Homo sapiens Infant, Newborn Male Pelvic Organ Prolapse Pregnancy Rupture, Spontaneous Ultrasonography, Prenatal Urachal Cyst Urinary Bladder Diseases
5
(4.0%)
28746173
(5627799)
Ultrasonographic diagnosis and minimally invasive treatment of a patent urachus associated with a patent omphalomesenteric duct in a newborn: A case report.
Bertozzi M, Recchia N, Di Cara G, Riccioni S, Rinaldi VE, Esposito S, Appignani A.
Medicine (Baltimore). 2017;96(30):e7087.
Granuloma
Homo sapiens Infant, Newborn Laparoscopy Male Minimally Invasive Surgical Procedures Ultrasonography Urachus
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 26

HPO ID Term # of case reports
HP:0030754 Allantoic cyst 7
HP:0000969 Edema 4
HP:0025615 Abscess 3
HP:0030654 Umbilical cord cyst 2
HP:0000021 Megacystis 1
HP:0000047 Hypospadias 1
HP:0000048 Bifid scrotum 1
HP:0000076 Vesicoureteral reflux 1
HP:0000126 Hydronephrosis 1
HP:0000252 Microcephaly 1
HP:0000347 Micrognathia 1
HP:0000506 Telecanthus 1
HP:0000581 Blepharophimosis 1
HP:0000796 Urethral obstruction 1
HP:0001195 Single umbilical artery 1
HP:0001369 Arthritis 1
HP:0001537 Umbilical hernia 1
HP:0001847 Long hallux 1
HP:0002014 Diarrhea 1
HP:0002664 Neoplasm 1
HP:0002982 Tibial bowing 1
HP:0004383 Hypoplastic left heart 1
HP:0012620 Cloacal abnormality 1
HP:0030868 Monorchism 1
HP:0031274 Hypovolemic shock 1
HP:0100548 Exstrophy 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID