LUCEY-DRISCOLL SYNDROME Mutations in the same gene cause Crigler- Najjar syndrome types I and II (, ) and Gilbert syndrome (). Disease name; Orpha number Synonym(s). Lucey-Driscoll syndrome An Orphanet summary for this disease is currently under development. However. Nonphysiologic neonatal jaundice – Maternal serum jaundice, also known as Lucey-Driscoll syndrome, is an autosomal recessive metabolic.
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When breastfeeding was stopped, the serum bilirubin levels began to decrease in all cases, but when breastfeeding was resumed, the serum bilirubin concentration again became elevated in some infants.
Research Publications Inherited disorders of bilirubin clearance. Goldman L, Schafer AI, eds. Educational Resources Added By: This is a list of diseases starting driscoll the letter “L”. Please help to improve this article by introducing more precise citations.
A substance, probably a metabolite of gestational hormones inhibitor of uridine diphosphate [UDP]-glucuronosyltransferase activitythat inhibits bilirubin conjugation is responsible for the disease.
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List of ICD-9 codes — Member feedback about List of syndromes: This information is not intended to be patient education, does not create any patient-physician relationship, and should not be used as a substitute for professional diagnosis and treatment. Views Read Edit View history. Clinical Sports Medicine Collection. Certain conditions originating in the perinatal period — Maternal causes of perinatal morbidity and mortality — Fetus or newborn affected by material conditions which may be unrelated to present pregnancy Check this box if you wish to receive a copy of your message.
Prognosis – Dgiscoll Driscoll syndrome Not supplied. The disorder is inherited in an autosomal recessive manner.
Lucey Driscoll syndrome — CheckOrphan
Lucey—Driscoll syndrome topic Lucey—Driscoll syndrome is an autosomal ulcey metabolic disorder affecting enzymes involved in bilirubin metabolism. Click the menu on the left to find more!
Member feedback about List of diseases L: Late neurodevelopmental or hearing defects were not observed, thus enabling the pediatrician to encourage continuation of breastfeeding in most cases of healthy infants with breast milk jaundice. Exclude other causes of hyperbilirubinemia, such as sepsis, driscol disease of the newborn, and biliary atresia. A rare condition characterized by severe jaundice at birth and caused by the presence of a gestational hormone that wyndrome from the mother to the infant across the placenta but eventually disappears after birth.
Crigler-Najjar syndrome, type II. Ask A Health Librarian. Rare conditions Genetic, autosomal recessive Congenital onset. Pediatrics Revolvy Brain revolvybrain. TEXT A number sign is used with this entry because of evidence that transient familial neonatal hyperbilirubinemia can be caused by heterozygous or homozygous mutation in the uridine diphosphate-glucuronosyltransferase gene UGT1A1; on chromosome 2q There are other causes for jaundice in the newborn that are easily treated.
It occurs when the body does not properly break down metabolize a certain form of bilirubin.
Lucey Driscoll syndrome
Treatment – Lucey Driscoll syndrome Not supplied. In infants with uninterrupted breastfeeding, the hyperbilirubinemia disappeared driacoll and could still be detected 12 weeks after birth. Search within a content type, and even narrow to one or more resources.
Displaying of 3 results. Transient familial neonatal hyperbilirubinemia.
Please enter User Name. Crigler-Najjar syndrome, type I. An Orphanet summary for this disease is currently under development. Drizcoll A rare condition characterized by severe jaundice at birth and caused by the presence of a gestational hormone that passes from the mother to the infant across the placenta but eventually disappears after birth.
The material is llucey no way intended to replace professional medical care by a qualified specialist and should not be used as a basis for diagnosis or treatment.