Pelger-Huët anomaly
... as pseudo-Pelger-Huët anomaly can be an early feature of myelodysplasia. "OMIM Entry - # 169400 - PELGER-HUET ANOMALY; PHA". ... Pelger-Huët anomaly)". Nature Genetics. 31 (4): 410-4. doi:10.1038/ng925. PMID 12118250. S2CID 6020153. "Pelger-Huet anomaly". ... Anomalies resembling Pelger-Huët anomaly that are acquired rather than congenital have been described as pseudo Pelger-Huët ... Pelger-Huet Anomaly at eMedicine (Articles with short description, Short description is different from Wikidata, Pages with ...
Neutrophilia
This can resemble Pelger-Huet anomaly. Absolute neutrophil count "neutrophilia" at Dorland's Medical Dictionary Table 12-6 in: ... Shmuely H, Pitlik SD, Inbal A, Rosenfeld JB (June 1993). "Pelger-Huët anomaly mimicking 'shift to the left'". Neth J Med. 42 (5 ...
Neutrophil-specific granule deficiency
Neutrophils and eosinophils will contain hyposegmented nuclei (a pseudo-Pelger-Huet anomaly). A majority of patients with SGD ...
Lamin B receptor
There is evidence tying it to Greenberg dysplasia and Pelger-Huet anomaly. Lamin B receptor has been shown to interact with ... "Deletion of LBR N-terminal domains recapitulates Pelger-Huet anomaly phenotypes in mouse without disrupting X chromosome ... Pelger-Huët anomaly)". Nature Genetics. 31 (4): 410-4. doi:10.1038/ng925. PMID 12118250. S2CID 6020153. Wells L, Vosseller K, ...
Polycomb recruitment in X chromosome inactivation
April 2021). "Deletion of LBR N-terminal domains recapitulates Pelger-Huet anomaly phenotypes in mouse without disrupting X ...
Australian Shepherd
Other conditions of note include iris coloboma, canine hip dysplasia, Pelger-Huet anomaly, hypothyroidism, and nasal solar ... Collie eye anomaly (CEA) is rare in the breed, but it and cataracts are a concern in Aussies. ... Retrieved July 5, 2007 "Collie Eye Anomaly (CEA)". Australian Shepherd Club of America, Inc. Archived from the original on July ...
Laminopathy
Pelger-Huet anomaly)". Nature Genetics. 31 (4): 410-4. doi:10.1038/ng925. PMID 12118250. S2CID 6020153. Captur, Gabriella; ... a single gene model for human Pelger-Huet anomaly". Human Molecular Genetics. 12 (1): 61-69. doi:10.1093/hmg/ddg003. ISSN 1460- ... "Deletion of LBR N-terminal domains recapitulates Pelger-Huet anomaly phenotypes in mouse without disrupting X chromosome ... Pelger-Huët anomaly)". Nature Genetics. 31 (4): 410-414. doi:10.1038/ng925. ISSN 1061-4036. PMID 12118250. S2CID 6020153. ...
Acrofrontofacionasal dysostosis
... and Pelger-Huet Anomaly syndrome and Infantile Liver Failure Syndrome.[citation needed] RESERVED, INSERM US14-- ALL RIGHTS. " ... and anomalies of foot structure.[citation needed] An association with mutations in the neuroblastoma amplified sequence gene ( ... "A previously undescribed autosomal recessive multiple congenital anomalies/mental retardation (MCA/MR) syndrome with fronto- ...
Stodtmeister cell
... s are a sub-classification of neutrophils exhibiting a Pelger-Huet anomaly with a non-lobed nucleus that may ...
List of MeSH codes (C15)
... pelger-huet anomaly MeSH C15.378.553.774 - phagocyte bactericidal dysfunction MeSH C15.378.553.774.257 - chediak-higashi ...
Myelodysplastic syndrome
... pseudo Pelger-Huet) Hypogranular neutrophils or pseudo Chediak-Higashi (large azurophilic granules) Auer rods - automatically ... other single or double anomalies Poor: complex (>3 chromosomal aberrations); chromosome 7 anomalies The IPSS is the most ... Jordans anomaly - vacuolization in all cell lines may be seen in Chanarin-Dorfman syndrome, aminolevulinic acid enzyme ...