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a deficiency of one of the enzymes of the urea cycle(passive) syndromes usually are caused byCongenital hyperammonemia
CHARGE syndrome ... all the conditionscausecongenital deafblindness
mutations in one of the three genes(passive) is caused byCongenital afibrinogenemia
a deficiency of enzyme cytochrome(passive) is caused byCongenital methemoglobinemia
a deficiency of enzyme(passive) is caused byCongenital methemoglobinemia
Deficiency of cytochrome b5 ... a rare disordercausescongenital methemoglobinemia
an inherited deficiency in the enzyme NADH - cytochrome b5 reductase , which is responsible for reducing methemoglobin in the blood(passive) is typically caused byCongenital methemoglobinemia
a rare disordercausescongenital methemoglobinemia
a genetic defect that you inherit from your parents(passive) is caused byCongenital methemoglobinemia
in a few the iron atom is oxidizedcausingcongenital methemoglobinemia
in some the iron atom is oxidizedcausingcongenital methemoglobinemia
neonatal infectionmay ... causecongenital dacryocystitis
Certain gene mutationscausingcongenital hypfibrinogenemia
abnormalities in the airways that cause them to partially(passive) is caused byCongenital stridor
A person is knownto causecongenital deafblindness
in certain the iron atom is oxidizedcausingcongenital methemoglobinemia
mutations in the V2R gene(passive) can be caused byCongenital NDI
abnormalities in the airways that cause them to partially collapse when the child breathes(passive) is caused byCongenital stridor
by an Arg275His mutation in the gamma chain of fibrinogen(passive) caused bycongenital dysfibrinogenemia
an Arg275His mutation in the gamma chain of fibrinogen(passive) caused bycongenital dysfibrinogenemia
mutations in the AVPR2 or the AQP2 genes(passive) is caused byCongenital NDI
by a mutation in the AQP2 gene(passive) could ... be causedcongenital NDI
by a mutation in the AQP2 gene(passive) could ... be caused bycongenital NDI
by V2R mutations(passive) caused bycongenital NDI
inherited defects in the genes encoding the vasopressin V2 receptor or the AQP2 water channel(passive) is caused byCongenital NDI
AVPR2 mutationcan causecongenital NDI
Toxoplasma gondii , rubella , or cytomegalovirus infections(passive) can be caused byCongenital chorioretinitis
mainly(passive) is ... causedCongenital NDI
degenerative and inflammatory processes(passive) is often caused byCongenital microphthalmia
by hemivertebra(passive) caused bycongenital kyphoscoliosis
usually(passive) is ... causedCongenital hypotonia
a defect that was present at birth(passive) is caused byCongenital skoliosis
any drugcausingCONGENITAL CHOROIDAL
The homozygous state of these enzymes deficiencycausescongenital methaemoglobinemia
the abnormal development of the arteriovenous plexus in the embryo(passive) are caused byCongenital AVMs
when an infected mother passes CMV virus to the fetus through the placenta(passive) is causedCongenital cytomegalovirus
Today ( 2006 ) , at least 20 different genetic syndromes are mittee on disability who in 1980 stated as follows : A person is knownto causecongenital deafblindness
a defect in compaction of muscle fibers during fetal development(passive) is caused byCongenital NCCM
com- Today ( 2006 ) , at least 20 different genetic syndromes are mittee on disability who in 1980 stated as follows : A person is knownto causecongenital deafblindness
oftenresultsoften
dyspneamay causedyspnea
abnormal hair growth on the face and bodycausesabnormal hair growth on the face and body
from a defective fibrinogen synthesis in the liverresultsfrom a defective fibrinogen synthesis in the liver
cholinergic deficiency(passive) caused bycholinergic deficiency
colour blindnesscausescolour blindness
to stress on the parscan leadto stress on the pars
to stress on the pars interarticulariscan leadto stress on the pars interarticularis
stress on the pars interarticulariscan causestress on the pars interarticularis
muscle weaknesscausesmuscle weakness
from prenatal weakness and associated lack of movementresultfrom prenatal weakness and associated lack of movement
CMV ) infectionresultsCMV ) infection
idiopathic scoliosiscausingidiopathic scoliosis
CMVresultsCMV
from abnormal chromosomesresultfrom abnormal chromosomes
in low vision and an abnormal appearance to my right eyeresultedin low vision and an abnormal appearance to my right eye
during the first month of lifediscoveredduring the first month of life
kidney cyst(passive) is caused bykidney cyst
from aberrations in neural crest cell growth ... differentiation and/or migrationmay resultfrom aberrations in neural crest cell growth ... differentiation and/or migration
from an epidermoid formation in the anterior superior lateral tympanic cavity adjacent to the anterior annulus during fetal developmentmay originatefrom an epidermoid formation in the anterior superior lateral tympanic cavity adjacent to the anterior annulus during fetal development
from abnormal chromosomes and also acquired lymphangioma that are the result of trauma or inflammationresultfrom abnormal chromosomes and also acquired lymphangioma that are the result of trauma or inflammation
from abnormal calcium metabolism in epidermal keratinocytesdirectly resultingfrom abnormal calcium metabolism in epidermal keratinocytes
feeding or respiratory compromisecan causefeeding or respiratory compromise
muscle weakness and fatigability similar to those of MGcausemuscle weakness and fatigability similar to those of MG
inflammation of the sacroiliac joint and have always had trouble standing or sittingcausesinflammation of the sacroiliac joint and have always had trouble standing or sitting