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an aberrant cross - linking of bone collagen ... due to underhydroxylation of lysine residues within the telopeptides of type I collagen(passive) is caused byPathogenesis Bruck syndrome
Other diseasescauseGrierson - Gopalan syndrome
a viral infectioncan causesTzeites syndrome
a deletion on the long arm of chromosome 15 that spans at least 7 genes(passive) is caused by15q13.3 microdeletion syndrome
by mutations in RAB27A(passive) caused byGriscelli syndrome
by the RAB27A mutation(passive) caused byGriscelli syndrome
a defect in one of three genes(passive) is caused byGriscelli Syndrome
More than 200 mutations in the HPRT1 gene have been foundto causeLesch - Nyhan syndrome
an abnormal gene(passive) is caused byCrigler - Najjar syndrome
by an abnormal gene(passive) is caused byCrigler - Najjar syndrome
At least one mutation in the MLPH gene has been foundto causeGriscelli syndrome
a liver enzyme deficiency(passive) is caused byCrigler - Najjar Syndrome
other drugscauseKOUNIS SYNDROME
a defect in the conjugation of bilirubin in the liver(passive) is caused byCrigler - Najjar syndrome
by an abnormal gene which fails to(passive) is caused bycrigler - najjar syndrome
by an abnormal gene which fails to (passive) is caused bycrigler - najjar syndrome
by an abnormal gene which fails to(passive) is causedcrigler - najjar syndrome
by an abnormal gene which fails to (passive) is causedcrigler - najjar syndrome
an abnormal gene which fails to produce a(passive) is caused byCrigler - Najjar syndrome
by bevacizumab(passive) caused byleukoencephalopathy syndrome
type 1(passive) is causedCrigler Najjar syndrome
a disorder in the metabolism of bilirubin , the chemical that causes jaundice(passive) is caused byCrigler - Najjar syndrome
a gene mutation that leads to overproduction of uric acid in the body(passive) is caused byLesch - Nyhan Syndrome
mast cell activationcausesKounis Syndrome
LRIG2 mutationscauseurofacial syndrome
by moderate decreases or absence of glucuronyl(passive) caused byCrigler Najjar syndrome
Mutations in HPSE2causeurofacial syndrome
an abnormal gene which fails to produce a functional enzyme ( bilirubin glucuronyltransferase ) capable of converting bilirubin into a water - soluble and(passive) is caused byCrigler - Najjar syndrome
by an abnormal gene which fails to produce a functional enzyme ( bilirubin glucuronyltransferase ) capable of converting bilirubin into a water - soluble and(passive) is causedCrigler - Najjar syndrome
by an abnormal gene which fails to produce a functional enzyme ( bilirubin glucuronyltransferase ) capable of converting bilirubin into a water - soluble and(passive) is caused byCrigler - Najjar syndrome
by moderate decreases or absence of glucuronyl transferase(passive) caused byCrigler Najjar syndrome
moderate decreases or absence of UDP glucuronyl transferase(passive) caused byCrigler - Najjar syndrome
by an abnormal gene which fails to produce a functional enzyme ( bilirubin glucuronyltransferase ) capable of converting bilirubin into a water - soluble and therefore , easily excreted form(passive) is caused byCrigler - Najjar syndrome
by an abnormal gene which fails to produce a functional enzyme ( bilirubin glucuronyltransferase ) capable of converting bilirubin into a water - soluble and therefore , easily excreted form(passive) is causedCrigler - Najjar syndrome
an abnormal gene which fails to produce a functional enzyme ( bilirubin glucuronyltransferase ) capable of converting bilirubin into a water - soluble and therefore , easily excreted form(passive) is caused byCrigler - Najjar syndrome
Increased level of AndrogenscausesVirilizing syndrome
by disrupted IFT - A - mediated retrograde ciliary transport(passive) is caused bySensenbrenner syndrome
disrupted IFT - A - mediated retrograde ciliary transport(passive) is caused bySensenbrenner syndrome
Kent bundles that connect the atrial and ventricular myocardium at some point around the valve annuli(passive) is caused byWFW syndrome
all kinds of seafood , such as finned fish , molluscan shellfish , cephalopods , and crustacean shellfish(passive) can also be caused byKounis syndrome
catastrophic seizurescan causecatastrophic seizures
oligaemia leading to and second andcausingoligaemia leading to and second and
irregular bowel complicationscan causeirregular bowel complications
alsocausesalso
overproduction of uric acidcauseoverproduction of uric acid
hundreds of basal cell tumors to develop over their lifetimecauseshundreds of basal cell tumors to develop over their lifetime
basal cell cancerscausesbasal cell cancers
people to bite themselvesmay causepeople to bite themselves
from heterozygous mutations in the PTCH1 generesultsfrom heterozygous mutations in the PTCH1 gene
an increased risk of developing cancers of the skin andcausesan increased risk of developing cancers of the skin and
an excess of uric acid in the body , resulting in kidney and bladder stones , and gouty arthritiscausesan excess of uric acid in the body , resulting in kidney and bladder stones , and gouty arthritis
jaundicecausesjaundice
to childhood gout or adenosine phosphoribosyltransferase deficiencyleadingto childhood gout or adenosine phosphoribosyltransferase deficiency
fatiguemay causefatigue
oral Quetiapine intakesetoral Quetiapine intake
oral Quetiapine intake ( to sleepsetoral Quetiapine intake ( to sleep
unconjugated hyperbilirubinemiacausesunconjugated hyperbilirubinemia
the top of the femur Femur The femur , or thigh bonecausesthe top of the femur Femur The femur , or thigh bone
blood vessels , pigment , and scar tissue to grow in and on the surface of the eyecausesblood vessels , pigment , and scar tissue to grow in and on the surface of the eye
paralysis of all muscles , which can lead to deathcausesparalysis of all muscles , which can lead to death
droopy upper eyelidscausesdroopy upper eyelids
the topcausesthe top
the top of the femur ( thigh bone ) to degeneratecausesthe top of the femur ( thigh bone ) to degenerate
kernicterus , which must be treatedcan causekernicterus , which must be treated
from a hereditary deficiency of the UDPG - transferase enzymeresultsfrom a hereditary deficiency of the UDPG - transferase enzyme
the neurological impairment(passive) caused bythe neurological impairment
the top of the femur ( thigh bone ) to degenerate , occurs in Yorkies in certain linescausesthe top of the femur ( thigh bone ) to degenerate , occurs in Yorkies in certain lines
from a transient dysfunction of RPE , which can occur as a post viral reactionresultsfrom a transient dysfunction of RPE , which can occur as a post viral reaction
to heart problemscan eventually leadto heart problems
her to have shorter limbs and to grow at a slower rate than other children , as well as experiencing liver and kidney problemscausesher to have shorter limbs and to grow at a slower rate than other children , as well as experiencing liver and kidney problems
to serious complicationscan leadto serious complications
cleft lip and palate , Hydronephrosis , Intestinal obstruction and other symptomscan causecleft lip and palate , Hydronephrosis , Intestinal obstruction and other symptoms
cleft lip and palate , Hydronephrosis , Intestinal obstruction and othercan causecleft lip and palate , Hydronephrosis , Intestinal obstruction and other
to multiple basal cell carcinomas of early onset ... and X - linked dominant chondrodysplasia punctata ( see these terms ) in which follicular atrophoderma may also be observedleadsto multiple basal cell carcinomas of early onset ... and X - linked dominant chondrodysplasia punctata ( see these terms ) in which follicular atrophoderma may also be observed
significant morbidity including self - inflicted oral hemorrhage ... and the necessary emergent measures are not easily decidedcan causesignificant morbidity including self - inflicted oral hemorrhage ... and the necessary emergent measures are not easily decided