LUCEY DRISCOLL PDF
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. 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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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 For all other comments, please send your remarks via contact us.
Lucey-driscoll Syndrome (disorder): Disease Bioinformatics
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Sulfonamides, ceftriaxone, pancuronium, and chloral hydrate are associated with hyperbilirubinemia. 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 lucy a milk component that inhibits uridine diphosphoglucuronic acid UDPGA glucuronyl transferase, thus resulting in a prolonged unconjugated hyperbilirubinemia.
Member feedback about UDP glucuronosyltransferase 1 family, polypeptide A1: Each first exon encodes the substrate binding site, and is regulated by its own promoter.
Lucey Driscoll syndrome
Lucey—Driscoll syndrome topic Lucey—Driscoll syndrome is an autosomal recessive metabolic disorder affecting enzymes involved in bilirubin metabolism. The mothers do not show hyperbilirubinemia, probably because of a large functional reserve. D ICD – From Wikipedia, the free encyclopedia. Displaying of 3 results.
OMIM Entry – # – HYPERBILIRUBINEMIA, TRANSIENT FAMILIAL NEONATAL; HBLRTFN
Transient familial neonatal hyperbilirubinemia. Crigler-Najjar syndrome, type II. Only comments written in English can be processed. Check this box if you wish to receive a copy of your message. Excessive jaundice result in kernicterus can cause complications such as brain damage.
Drugs that interfere with metabolism of bilirubin or that may displace bilirubin from albumin could increase the risk of hyperbilirubinemia or kernicterus. Crigler—Najjar syndrome or CNS is a rare inherited disorder affecting the metabolism of bilirubin, a chemical formed from the breakdown of the heme in red blood cells. Disease Resources Resources can help guide driscol quest lucsy factual and reliable information. Dubin—Johnson syndrome Rotor syndrome.
Serum from these mothers contains no more inhibitory substance than does normal pregnancy serum. Please enter Password Forgot Username?
Support Organizations Support organizations can provide help and guidance in areas such as peer drisfoll, education and training, and therapy and counseling. 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.
Info Lucey Driscoll syndrome.
The cause of driiscoll neonatal hyperbilirubinemia may be steroidal substances in the plasma and milk of the mother that inhibit conjugation of bilirubin Lucey et al. Expert curators review the literature and organize it to facilitate your work.
This section is empty. The inhibitor is probably a progestational steroid.
Lucey Driscoll syndrome — CheckOrphan
Hereditary coproporphyria Harderoporphyria Variegate porphyria Erythropoietic protoporphyria. Hyperbilirubinemia, familial transient neonatal. Rare conditions Genetic, autosomal recessive Congenital onset.
Health care resources for this disease Expert centres 69 Diagnostic tests 7 Patient organisations 22 Orphan drug s 0. This syndrome is divided into types I and II, with the latter sometimes called Arias syndrome. Kernicterus has not been observed, probably because severe jaundice does not develop until the seventh to tenth day, when the infant’s blood-brain barrier has become relatively impermeable to unconjugated bilirubin Arias et al.
Educational Resources Added By: The same condition may be present in unusually high frequency in Yemenite Jews Sheba, All siblings are usually affected, and there is frequently a history of the phenomenon occurring in previous generations.