PALABRAS DEL INGLÉS RELACIONADAS CON «SPHEROCYTOSIS»
spherocytosis
symptoms
pregnancy
hereditary
osmotic
fragility
test
treatment
causes
mchc
patient
information
spherocytosis
auto
hemolytic
anemia
characterized
production
blood
cells
erythrocytes
that
genetics
home
reference
condition
affects
people
with
typically
experience
shortage
diagnosis
treatments
disorder
membrane
your
like
medscape
familial
marked
heterogeneity
clinical
features
ranging
from
asymptomatic
seattle
children
hospital
child
fragile
easily
destroyed
level
means
body
does
medical
definitions
genetic
clinically
jaundice
yellowing
splenomegaly
department
pediatrics
abnormality
while
healthy
flattened
indented
10 LIBROS DEL INGLÉS RELACIONADOS CON «SPHEROCYTOSIS»
Descubre el uso de
spherocytosis en la siguiente selección bibliográfica. Libros relacionados con
spherocytosis y pequeños extractos de los mismos para contextualizar su uso en la literatura.
1
Oral Diagnosis, Oral Medicine, and Treatment Planning
The congenital hemolytic anemias can be further classified as membrane defects
(e.g., hereditary spherocytosis), enzyme deficiencies (e.g., G-6-PD deficiency and
pyru- vate kinase deficiency), and disorders of hemoglobin (e.g., sickle cell ...
Steven L. Bricker, B C Decker, Robert P. Langlais, 2001
TABLE 25-7 TYPES OF ANEMIAS Nutritional Iron deficiency Vitamin B12
deficiency Folic acid deficiency Chronic illness Hemolytic Spherocytosis Glucose
-6-phosphate dehydrogenase deficiency Immune-mediated Drug-induced ABO ...
3
Anesthesia for Genetic, Metabolic, and Dysmorphic Syndromes ...
Hereditary spherocytosis. A young boy with congenital spherocytosis posing with
his gallstones following a chole- cystectomy and partial splenectomy. His
hematocrit was 22 and his total bilirubin 10.4 mg/dL (direct fraction 0.8 mg/dL).
loss of ...
Victor C. Baum, Jennifer E. O'Flaherty, 2007
4
Hematology: Clinical Principles and Applications
Eber SW, Gonzalez JM, Lux ML, et al: Ankyrin-1 mutations are a major cause of
dominant and recessive hereditary spherocytosis. Nat Genet 1996;13:214-218.
18. Alloisio N, Texier P, Vallier A, et al: Modulation of clinical expression and
band ...
5
Spherocytosis: New Insights for the Healthcare Professional: ...
The researchers concluded: “While a similar deletion has previously been
reported in a family with spherocytosis, severe learning disabilities, and mild
mental retardation, this is the first implication of chr14q23.2-23.3 in the etiology of
autism ...
6
Hemorheology in Practice
7.3.2 Changes of Membrane Shape or Constitutional Deficiency of the
Membrane Spherocytosis Spherocytosis is one of the congenital hemolytic
anemias whose biological diagnosis has for some time been based on a
rheological criterion ...
J. F. Stoltz, Megha Singh, Pavel Riha, 1999
Both hereditary spherocytosis and hereditary elliptocytosis are associated with
neonatal hemolysis. Hereditary spherocytosis Hereditary spherocytosis is the
most common of the hereditary hemolytic anemias among people of Northern ...
Pedro A. de Alarcón, Eric J. Werner, 2005
8
Red Blood Cell Membranes: Structure: Function: Clinical ...
Structure: Function: Clinical Implications Peter Agre. III. HEREDITARY
SPHEROCYTOSIS Hereditary spherocytosis (HS) has been estimated to occur
with a frequency of ~25 per 100,000 population in the northern United States and
England ...
9
Wintrobe's Clinical Hematology
'By definition, patients with severe spherocytosis are transfusion-dependent.
Normal ( ± SD) = 245 ± 27 x 105 spectrln dimers per eiythrocyte. In most patients,
ankyrin content is decreased to a comparable degree. A minority of HS patients ...
10
Medical Knowledge Self-assessment Program for Students Four
[PMID: 17217902] Item 6 Answer: A This patient's peripheral blood smear shows
evidence of hereditary spherocytosis, a disorder of the skeletal membrane
proteins in the red blood cell. The most appropriate next diagnostic step is to
review ...
American College of Physicians, 2008
10 NOTICIAS EN LAS QUE SE INCLUYE EL TÉRMINO «SPHEROCYTOSIS»
Conoce de qué se habla en los medios de comunicación nacionales e internacionales y cómo se emplea el término
spherocytosis en el contexto de las siguientes noticias.
Lilli's death preventable: Qld family
In June 2011, Lilli Sweet, then aged four-and-a-half, underwent a splenectomy, or removal of the spleen, to address her Spherocytosis. Lilli's father and ... «9news.com.au, Jul 15»
Nambour Hospital to be put under microscope for inquest into six …
Lilli was born on December 4, 2006, and found to have hereditary spherocytosis. Those with this condition experience a shortage of red blood cells, yellowing of ... «Courier Mail, Jul 15»
Material Contribution - Case Update: ST V Maidstone (2015)
The Claimant suffered congenital haematological conditions including hereditary spherocytosis. The level of haemoglobin (Hb) in the blood for an average child ... «Mondaq News Alerts, Jun 15»
ASU's Shelby Houlihan goes for 2nd NCAA 1500-meter title
She had her spleen and gallbladder removed when she was eight because of spherocytosis, a hereditary blood disorder affecting red blood cells. Without her ... «azcentral.com, Jun 15»
To Your Good Health: Hospice switches focus from quantity to quality
Some genetic conditions, like hereditary spherocytosis, can do it. Even low thyroid levels sometimes can cause large red blood cells and a high MCV. «TwinCities.com-Pioneer Press, May 15»
16-year-old girl with blood disorder plays a dream round with Rory
Grace Vaughan is 16-years-old and has a rare blood disorder called hereditary spherocytosis. She says her disorder always made it tough to fit in and rattled ... «USA TODAY, May 15»
Upstate teen tees off with Rory McIlroy
Grace Vaughan, 16, was born with hereditary spherocytosis and lacked the stamina of most kids. At the age of 7, Vaughan discovered Camp Courage, ... «WHNS Greenville, May 15»
State of Grace: Young golfer in spotlight with McIlroy
She provided two lengthy answers that included dealing hereditary spherocytosis – a rare blood disorder that forced multiple transfusions at 3-years-old and the ... «Spartanburg Herald Journal, May 15»
Infection-fighting service introduced to Queensland patients
He has a hereditary blood illness – hereditary spherocytosis – which in layman's terms is an abnormality of the red blood cell causing severe anaemeia. «Brisbane Times, May 15»
SSA issues final rules revising its criteria for evaluating …
Adding hereditary spherocytosis to the list of common examples of hemolytic anemias in adults upon a commenter's recommendation. Hereditary spherocytosis ... «CCH, May 15»
