Biomaterial Database

Pelger-Huët anomaly. 1981

B N Agarwala, and C Green, and H B Levy

UI	MeSH Term	Description	Entries
D007223	Infant	A child between 1 and 23 months of age.	Infants
D008297	Male		Males
D010381	Pelger-Huet Anomaly	Autosomal dominant anomaly characterized by abnormal ovoid shape GRANULOCYTE nuclei and their clumping chromatin. Mutations in the LAMIN B receptor gene that results in reduced protein levels are associated with the disorder. Heterozygote individuals are healthy with normal granulocyte function while homozygote individuals occasionally have skeletal anomalies, developmental delay, and seizures.	Ovoid Neutrophil Nuclei, Developmental Delay, Epilepsy and Skeletal Abnormalities,Ovoid Neutrophil Nuclei, Developmental Delay, Epilepsy, and Skeletal Abnormalities,Pelger-Huet Nuclear Anomaly,Pelger-Huët Anomaly,Pelger-Huët Nuclear Anomaly,Pseudo Pelger-Huet Anomaly,Pseudo Pelger-Huet Nuclear Anomaly,Pseudo Pelger-Huët Anomaly,Anomaly, Pelger-Huet,Anomaly, Pelger-Huet Nuclear,Anomaly, Pelger-Huët,Anomaly, Pelger-Huët Nuclear,Anomaly, Pseudo Pelger-Huet,Anomaly, Pseudo Pelger-Huët,Nuclear Anomaly, Pelger-Huet,Nuclear Anomaly, Pelger-Huët,Pelger Huet Anomaly,Pelger Huet Nuclear Anomaly,Pelger Huët Anomaly,Pelger Huët Nuclear Anomaly,Pelger-Huet Anomaly, Pseudo,Pelger-Huët Anomaly, Pseudo,Pseudo Pelger Huet Anomaly,Pseudo Pelger Huet Nuclear Anomaly,Pseudo Pelger Huët Anomaly
D002675	Child, Preschool	A child between the ages of 2 and 5.	Children, Preschool,Preschool Child,Preschool Children
D006801	Humans	Members of the species Homo sapiens.	Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man