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searching for Pancytopenia 24 found (117 total)
alternate case: pancytopenia
Fanconi syndrome
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Fanconi syndrome or Fanconi's syndrome (English: /fɑːnˈkoʊni/, /fæn-/) is a syndrome of inadequate reabsorption in the proximal renal tubules of the kidneyDurvalumab (2,734 words) [view diff] exact match in snippet view article find links to article
interstitial lung disease, pancytopenia, and sepsis [n=1 each]), and two (1%) in the platinum–etoposide group (pancytopenia and thrombocytopenia [n=1 each])Follow the Legion (318 words) [view diff] exact match in snippet view article find links to article
Hunter-Mellado, Robert (2015-12-22). "Profile of HIV-Infected Hispanics with Pancytopenia". International Journal of Environmental Research and Public Health.Sphingolipidoses (652 words) [view diff] exact match in snippet view article find links to article
Glucocerebrosidase Glucocerebrosides in RBCs, liver and spleen Hepatosplenomegaly Pancytopenia Bone pain Erlenmeyer flask deformity Autosomal recessive About 1 in 20Thiopurine methyltransferase (1,455 words) [view diff] exact match in snippet view article find links to article
Schütz E, Haas JP, Oellerich M (1997). "Azathioprine-induced severe pancytopenia due to a homozygous two-point mutation of the thiopurine methyltransferaseMacrolide (2,795 words) [view diff] exact match in snippet view article find links to article
colchicine toxicity include gastrointestinal upset, fever, myalgia, pancytopenia, and organ failure. Arriola Apelo SI, Lamming DW (July 2016). "apamycin:Dyskerin (1,127 words) [view diff] exact match in snippet view article find links to article
case of a separate entity with prenatal growth retardation, progressive pancytopenia and cerebellar hypoplasia". Eur. J. Pediatr. 154 (4): 304–8. doi:10.1007/BF01957367List of diseases (F) (924 words) [view diff] exact match in snippet view article
syndrome Fanconi ichthyosis dysmorphism Fanconi like syndrome Fanconi pancytopenia Fanconi syndrome Fanconi syndrome, renal, with nephrocalcinosis and renalDPP9 (973 words) [view diff] exact match in snippet view article find links to article
in DPP9 with a phenotype of failure to thrive, skin manifestations, pancytopenia, and susceptibility to infections. This gene has also been linked toProton-coupled folate transporter (2,649 words) [view diff] exact match in snippet view article find links to article
macrocytic, always accompanies the folate deficiency. Sometimes there is pancytopenia and/or hypogammaglobulinemia and/or T-cell dysfunction which can resultLetterer–Siwe disease (1,233 words) [view diff] exact match in snippet view article find links to article
present with hemorrhage and sepsis secondary to hepatic failure and severe pancytopenia. A purpuric rash or bruise may be apparent right before death in a patientMalignant infantile osteopetrosis (699 words) [view diff] exact match in snippet view article find links to article
Hematologic manifestations related to bone marrow suppression and subsequent pancytopenia are a major source of morbidity and mortality. Additionally, extramedullaryCopper deficiency (2,727 words) [view diff] exact match in snippet view article find links to article
Wilcock, S.; London, Z.; Brewer, G.J. (2009). "Myelopolyneuropathy and pancytopenia due to copper deficiency and high zinc levels of unknown origin II. TheHoyeraal–Hreidarsson syndrome (570 words) [view diff] exact match in snippet view article find links to article
Hoyeraal–Hreidarsson syndrome Other names Progressive pancytopenia-immunodeficiency-cerebellar hypoplasia syndrome This condition is inherited in an X-linkedMelperone (1,291 words) [view diff] exact match in snippet view article find links to article
Tardive dyskinesia Neuroleptic malignant syndrome Blood dyscrasias (pancytopenia, agranulocytosis, leukopenia, thrombocytopenia, etc.) Unknown frequencyLangerhans cell histiocytosis (4,022 words) [view diff] exact match in snippet view article find links to article
of LCH patients have extensive eruptions on the scalp. Bone marrow: Pancytopenia with superadded infection usually implies a poor prognosis. Anemia canWilson's disease (5,003 words) [view diff] exact match in snippet view article find links to article
S2CID 205999334. Harper PL, Walshe JM (December 1986). "Reversible pancytopenia secondary to treatment with tetrathiomolybdate". Br. J. Haematol. 64Fanconi anemia, complementation group C (2,397 words) [view diff] exact match in snippet view article find links to article
1016/S0378-1119(97)00411-3. PMID 9373149. GeneReviews/NCBI/NIH/UW entry on 9q22.3 Microdeletion GeneReviews/NCBI/NIH/UW entry on Fanconi Anemia or PancytopeniaPolish plait (2,106 words) [view diff] exact match in snippet view article find links to article
"Plica Neuropathica (Plica polonica) Following Azathioprine-induced Pancytopenia". International Journal of Trichology. 2 (2): 110–2. doi:10.4103/0974-7753Azithromycin (5,711 words) [view diff] exact match in snippet view article find links to article
colchicine toxicity include gastrointestinal upset, fever, myalgia, pancytopenia, and organ failure. CYP3A4 is an enzyme that metabolizes many drugs inCotton wool spots (2,616 words) [view diff] exact match in snippet view article find links to article
due to its side effects of lymphopenia, neutropenia, thrombocytopenia, pancytopenia, and infections as well as the timing of the formation of cotton woolList of skin conditions (17,971 words) [view diff] exact match in snippet view article find links to article
benign pemphigus, Hailey–Hailey disease) Fanconi syndrome (familial pancytopenia, familial panmyelophthisis) Fibrodysplasia ossificans progressiva FocalDNA repair protein XRCC4 (5,681 words) [view diff] exact match in snippet view article find links to article
immunological phenotype. In contrast to individuals with a LIG4 mutation, pancytopenia resulting in bone marrow failure is not observed in individuals withCancer pharmacogenomics (4,062 words) [view diff] exact match in snippet view article find links to article
homozygous for the *2 and *3 alleles, can experience myelosuppression up to pancytopenia. In a study on 1214 European Caucasian individuals, a trimodal distribution