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Latest revision as of 16:37, 19 July 2016

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:

Overview

Lucey-Driscoll syndrome is an autosomal recessive metabolic disorder affecting enzymes involved in bilirubin metabolism. It is one of several disorders classified as a transient familial neonatal unconjugated hyperbilirubinemia.

Historical Perspective

Classification

Pathophysiology

Causes

The common cause is congenital, but it can also be caused by maternal steroids passed on through breast milk to the newborn. It is different from breast milk jaundice (breast-fed infants have higher bilirubin levels than formula-fed ones).

Differentiating Lucey-Driscoll syndrome from Other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications, and Prognosis

Natural History

Complications

Prognosis

Diagnosis

Genetics

File:Autorecessive.svg
A defect in the UGT1A1-gene, also linked to Crigler-Najjar syndrome and Gilbert's syndrome, is responsible for the congenital form of Lucey-Driscoll syndrome.

Diagnostic Criteria

History and Symptoms

Physical Examination

Laboratory Findings

Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Prevention

References

External Links

Online Mendelian Inheritance in Man (OMIM) 237900 - transient familial neonatal hyperbilirubinemia, breast feeding jaundice included
Hyperbilirubinemia, Unconjugated at eMedicine
Template:RareDiseases

Template:Heme metabolism disorders

Template:WS Template:WH

@@ Line 1: / Line 1: @@
-{{Infobox_Disease |
+__NOTOC__
-  Name           = Lucey-Driscoll syndrome |
+{{SI}}
-  Image          = |
+{{CMG}}; {{AE}}
-  Caption        = |
-  DiseasesDB     = 32677 |
-  ICD10          = |
-  ICD9           = {{ICD9|774.30}} |
-  ICDO           = |
-  OMIM           = 237900|
-  MedlinePlus    = |
-  eMedicineSubj  = |
-  eMedicineTopic = |
-  MeshID         = |
-}}
-'''Lucey-Driscoll syndrome''' is an [[autosomal recessive]] metabolic disorder affecting enzymes involved in [[bilirubin]] metabolism.
-It is one of several disorders classified as a transient familial neonatal unconjugated [[hyperbilirubinemia]].
+==Overview==
+'''Lucey-Driscoll syndrome''' is an [[autosomal recessive]] metabolic disorder affecting enzymes involved in [[bilirubin]] metabolism.  It is one of several disorders classified as a transient familial neonatal unconjugated [[hyperbilirubinemia]].
+==Historical Perspective==
-==Cause==
+==Classification==
+==Pathophysiology==
+==Causes==
 The common cause is congenital, but it can also be caused by maternal [[steroids]] passed on through [[breast milk]] to the [[newborn]]. It is different from breast milk jaundice (breast-fed infants have higher bilirubin levels than formula-fed ones).
+==Differentiating Lucey-Driscoll syndrome from Other Diseases==
+==Epidemiology and Demographics==
+==Risk Factors==
+==Screening==
+==Natural History, Complications, and Prognosis==
+===Natural History===
+===Complications===
+===Prognosis===
+==Diagnosis==
 ==Genetics==
-[[Image:autorecessive.svg|thumb|right|Lucey-Driscoll syndrome has an autosomal recessive pattern of inheritance.]]
+[[Image:autorecessive.svg|thumb|left|Lucey-Driscoll syndrome has an autosomal recessive pattern of inheritance.]]
+<br clear="left"/>
+A defect in the [[UGT1A1]]-gene, also linked to [[Crigler-Najjar syndrome]] and [[Gilbert's syndrome]], is responsible for the congenital form of Lucey-Driscoll syndrome.
-A defect in the [[UGT1A1]]-gene, also linked to [[Crigler-Najjar syndrome]] and [[Gilbert's syndrome]], is responsible for the congenital form of Lucey-Driscoll syndrome.
+===Diagnostic Criteria===
+===History and Symptoms===
+===Physical Examination===
+===Laboratory Findings===
+===Imaging Findings===
+===Other Diagnostic Studies===
+==Treatment==
+===Medical Therapy===
+===Surgery===
+===Prevention===
+==References==
+{{reflist|2}}
-==External links==
+==External Links==
 *{{OMIM|237900}} - transient familial neonatal hyperbilirubinemia, breast feeding jaundice included
 *{{eMedicine|med|1066|Hyperbilirubinemia, Unconjugated}}
@@ Line 34: / Line 66: @@
 [[Category:Hepatology]]
-[[Category:Genetic disorders]]
-[[Category:Autosomal recessive disorders]]
+{{WS}}
-[[Category:Syndromes]]
+{{WH}}