LUCEY-DRISCOLL SYNDROME. Other entities represented in this entry: BREAST MILK JAUNDICE, INCLUDED. Phenotype-Gene Relationships. Location. Lucey–Driscoll syndrome is an autosomal recessive metabolic disorder affecting enzymes involved in bilirubin metabolism.[1] It is one of several disorders. Lucey-Driscoll syndrome. Prevalence: ; Inheritance: ; Age of onset: Neonatal; ICD P; OMIM: ; UMLS: C; MeSH: ; GARD:

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If your institution subscribes to this resource, and you don’t have a MyAccess Profile, please contact your library’s reference desk for information on how to gain access to this resource from off-campus. Benign disorder of metabolism of bilirubin resulting in transient neonatal hyperbilirubinemia unconjugated bilirubin. Transient Familial Neonatal Hyperbilirubinemia. Usually all siblings are affected. Cases transmitted as an autosomal recessive trait gene map locus is 2q37 have been reported.

A substance, probably a metabolite driscol gestational hormones inhibitor of uridine diphosphate [UDP]-glucuronosyltransferase activitythat inhibits bilirubin conjugation is responsible for the disease.

This inhibitor is present in the sera of both mother and infant.

Lucey Driscoll syndrome — CheckOrphan

Unconjugated hyperbilirubinemia, which is more severe than the form observed in breast milk jaundice, is kucey.

The presence of significant neonatal jaundice frequently associated with a familial pattern.

All siblings are usually affected, and there is frequently a history of the phenomenon occurring in previous generations. Other causes of hyperbilirubinemia should be excluded. Unconjugated hyperbilirubinemia resulting in sriscoll usually presenting on the third to fifth day of life and persisting for 3 weeks.


Left untreated, kernicterus may develop.

Phototherapy is used to treat the hyperbilirubinemia. Exclude other causes of hyperbilirubinemia, such as sepsis, hemolytic disease of the newborn, and biliary atresia.

Lucey–Driscoll syndrome | Revolvy

Obtain coagulation profile and bleeding time. This syndrome occurs only in neonates; therefore, basic principles of safe neonatal anesthesia must be applied. Drugs that interfere with metabolism of bilirubin or that may displace bilirubin from albumin could increase the risk of hyperbilirubinemia or kernicterus.

Sulfonamides, ceftriaxone, pancuronium, and chloral hydrate are associated with hyperbilirubinemia. The hereditary hyperbilirubinemias include 1 those resulting in predominantly unconjugated hyperbilirubinemia, such as Gilbert or Arias syndrome, Crigler-Najjar syndrome type I, and Crigler-Najjar syndrome type II; and 2 those resulting in predominantly conjugated hyperbilirubinemia, such as Dubin-Johnson syndrome, Rotor syndrome, and other forms of intrahepatic cholestasis.

Jaundice occurring in breast-fed neonate around the fourth to seventh day of life, persisting beyond physiologic jaundice, and with no other identifiable cause, probably resulting from a milk component that inhibits uridine diphosphoglucuronic acid UDPGA glucuronyl transferase, thus resulting in a prolonged unconjugated hyperbilirubinemia.

Inherited error of bilirubin metabolism in which bilirubin cannot be converted into water-soluble bilirubin glucuronide because of a defect of hepatic glucuronyl transferase.

Crigler-Najjar syndrome type II is less severe than type I. Characterized by normal liver function tests, normal liver histology, delayed clearance of bilirubin from the blood, and mild jaundice that tends to fluctuate in severity, particularly after fasting. It is defined as a mild unconjugated hyperbilirubinemia resulting from a mutation in the promoter of the UDP-glucuronosyltransferase gene allelic to the mutation for Crigler-Najjar syndrome type I.


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Lucey-driscoll Syndrome (disorder): Disease Bioinformatics

Clinical Sports Medicine Collection. Search Advanced search allows to you precisely focus your query. Search within a content type, and even narrow to one or more resources. You can also find results for a single author kucey contributor. Rapid Recognition and Perioperative Implications. Bruno Bissonnette, et al.

Lucey Driscoll syndrome

Accessed December 31, Rare; 24 cases reported. Please enter User Name. View All Subscription Options. Pop-up div Successfully Displayed This div only appears when the trigger link is hovered over. This site uses cookies to provide, maintain and improve your experience.

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