- May-Hegglin anomaly
- May-Hegg·lin anomaly (miґ hegґlin) [Richard May, German physician, 1863–1936; Robert Marquard Hegglin, Swiss physician, 1907–1969] see under anomaly.
Medical dictionary. 2011.
May-Hegglin anomaly
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May-Hegglin anomaly — Classification and external resources ICD 10 D72.0 … Wikipedia
May Hegglin anomaly — Infobox Disease Name = PAGENAME Caption = DiseasesDB = 29517 ICD10 = ICD10|D|72|0|d|70 ICD9 = ICD9|288.2 ICDO = OMIM = 155100 MedlinePlus = eMedicineSubj = ped eMedicineTopic = 1383 MeshID = May Hegglin s anomaly, as it is also known, is a rare… … Wikipedia
May-Hegglin anomaly — an autosomal dominant disorder of blood cell morphology, caused by mutations in the MYH9 gene (locus: 22q11.2), which encodes a component of nonmuscle myosin. It is characterized by blue, RNA containing cytoplasmic inclusions similar to Dцhle… … Medical dictionary
May-Hegglin-Anomalie — Klassifikation nach ICD 10 D72.0[1] Genetisch bedingte Leukozytenanomalien … Deutsch Wikipedia
Anomaly — A deviation from the usual, something different, peculiar, or abnormal. A congenital anomaly is something that is unusual and different at birth. A minor anomaly in this context is defined as an unusual anatomic feature that is of no serious… … Medical dictionary
Hegglin — Robert M.P., Swiss physician, 1907–1970. See H. anomaly, H. syndrome, May H. anomaly … Medical dictionary
May — Richard, German physician. See M. Hegglin anomaly … Medical dictionary
Robert Hegglin — Infobox Scientist name = PAGENAME box width = image width =150px caption = PAGENAME birth date = 1907 birth place = death date = 1969 death place = residence = citizenship = nationality = Switzerland ethnicity = field = medicine work institutions … Wikipedia
Macrotrombocitopenias hereditarias — Las macrotrombocitopenias hereditarias son un grupo heterogéneo de enfermedades que asocian trombocitopenia y plaquetas gigantes. Pueden incluir todos o algunos de los siguientes rasgos clínicos: nefritis hereditaria, sordera neurosensorial,… … Wikipedia Español
MYH9 — Idiogramm des menschlichen Chromosom 22. MYH9 befindet sich auf Band q11.2 MYH9 (Myosin, heavy chain 9) ist ein Gen, welches sich beim Menschen auf Chromosom 22 Genlocus q11.2 befindet.[1][2][3] … Deutsch Wikipedia
