mutations in the CRLF1 gene(passive) is caused byCrisponi Syndrome
mutation in CRLF1 gene(passive) is caused byCrisponi syndrome
germline heterozygous loss - of - function sequence mutations within the mismatch repair genes MLH1 , MSH2 , MSH6 or PMS2(passive) is caused bysyndrome
by the triplication of more than 100 genes on human chromosome 21 , including the gene that encodes APP(passive) 's caused bysyndrome
pre - eclampsia or pregnancy poisoningmay resultin HELLP syndrome
Severe preeclampsiamay leadto HELLP syndrome
severe preeclampsiahad ... ledto HELLP syndrome
pregnancycausingHELLP syndrome
autosomal dominant mutations in the human fibrillin 1 gene ( FBN1 ) with de novo mutations occurring in about 25 % of cases(passive) is caused bysyndrome
having three copies of chromosome 21 , causing an extra copy of the APP gene(passive) is caused bySyndrome
infection with a specific virus from a group of viruses called hantavirus(passive) is caused bysyndrome
the presence of an extra copy of chromosome 21 in a baby?s cells(passive) is caused bysyndrome
Life with Down syndrome Down syndrome ... a genetic disorder Free essay on down ... mental retardation and physical it is caused by the presence of an extra copy of chromosome number 21causessyndrome
by mutations in the SCN1A sodium channel gene(passive) caused bysyndrome
any of at least five different mutations in the HRAS gene on chromosome 11(passive) is caused bysyndrome
As scientists do not knowcausesHELLP syndrome
by compound heterozygous mutations within the PMS2 gene(passive) caused bysyndrome
by the deletion ( a missing piece ) of genetic material on the small arm ( the p arm ) of chromosome 5(passive) is caused bysyndrome
Doctors do not knowcausesHELLP syndrome
mutations in the mismatch repair genes , e.g. , MLH1 , MSH2 , MSH6 , and PMS2(passive) can be caused bysyndrome
germline mutations in the PTEN gene(passive) is caused bysyndrome
autosomal dominant mutations in the human fibrillin-1 ( FBN1 ) gene(passive) is caused bysyndrome
by a recurrent de novo missense mutation in the fibrillin gene(passive) caused bysyndrome
the presence of an extra chromosome ( number 21 ) in the cells of a developing baby(passive) is caused bysyndrome
due to mutation of a single known present on the x chromosome(passive) is causedsyndrome
by the presence of an extra copy of chromosome 21 ( trisomy 21(passive) caused bySyndrome
The endothelial injurycausingthe HELLP syndrome
by mutations in the MECP2 gene(passive) are causedSyndrome
partial deletion of the short arm of one chromosome 4(passive) is caused bysyndrome
pre - eclampsiamay causeHELLP syndrome
pre - eclampsiacan leadto the HELLP Syndrome
mutations in AAAS , a new WD - repeat protein gene(passive) is caused bysyndrome
the presence of an extra X chromosome and an extra Y chromosome in a male 's cells(passive) is caused bysyndrome
by an extra copy of human chromosome 21(passive) is caused bysyndrome
by preeclampsia(passive) caused byHELLP Syndrome
the groupleadthe group
the body to destroy its own bloodcausesthe body to destroy its own blood
by over textingcausedby over texting
deathcausingdeath
as with any disorder of pregnancy causing liver dysfunctioncan resultas with any disorder of pregnancy causing liver dysfunction
problems with the liver , blood cells and blood clottingcausesproblems with the liver , blood cells and blood clotting
low platelets and elevated liver enzymescauseslow platelets and elevated liver enzymes
my liver enzymes to become elevatedcausedmy liver enzymes to become elevated
other problemscan causeother problems
The problems(passive) caused byThe problems
multiple organ failurehad causedmultiple organ failure
liver functions(passive) caused byliver functions
from a chronic problemresultingfrom a chronic problem
to a diagnosis of pregnancyleadingto a diagnosis of pregnancy
in fetal deathresultingin fetal death
hepatic rupture(passive) caused byhepatic rupture
to serious complications , including liver failure and deathcan leadto serious complications , including liver failure and death
from somatic dysfunctionresultingfrom somatic dysfunction
to liver failurecan leadto liver failure
in breakdown of red blood cells causing anemia and blood clotting problems leading to disseminated intravascular coagulationcan resultin breakdown of red blood cells causing anemia and blood clotting problems leading to disseminated intravascular coagulation
her liver to rupture in early laborcausedher liver to rupture in early labor
alsocan ... setalso
from gall bladder diseaseresultingfrom gall bladder disease
me to go into preterm laborcausedme to go into preterm labor
liver damagecan causeliver damage
the breaking down of red blood cells ... elevated liver enzymes or proteins and low platelet countcausesthe breaking down of red blood cells ... elevated liver enzymes or proteins and low platelet count
problems with your blood , liver , and blood pressurecausesproblems with your blood , liver , and blood pressure
your neck painis causingyour neck pain
premature birthcan causepremature birth
to neuropathy avoidleadto neuropathy avoid
life - threatening liver damage , gestational diabetes , anemia , and blood clotscan causelife - threatening liver damage , gestational diabetes , anemia , and blood clots
severe development delays due to an extra chromosome 18causessevere development delays due to an extra chromosome 18
severe developmental delays due to an extra chromosomecausessevere developmental delays due to an extra chromosome
an irresistible urge to move the legs with its uncomfortable , tingling , aching or creeping sensationscausesan irresistible urge to move the legs with its uncomfortable , tingling , aching or creeping sensations
a variety of medical and developmental problems , including short height , failure of the ovaries to develop and heart defectscan causea variety of medical and developmental problems , including short height , failure of the ovaries to develop and heart defects
to acute , severe renal and pulmonary problemsleadsto acute , severe renal and pulmonary problems
mental retardation in the children and they have very characteristic physical features that is only associated with this disordercausesmental retardation in the children and they have very characteristic physical features that is only associated with this disorder
a distinct facial appearance , intellectual disability , developmental delays and other physical challengescausesa distinct facial appearance , intellectual disability , developmental delays and other physical challenges
menstrual abnormalities , including painful cycles , infertility or miscarriagecan causemenstrual abnormalities , including painful cycles , infertility or miscarriage