# Clinical-Pathological Conference Series from the Medical University of Graz: Case No 178: A 30-year-old nurse with urine dipstick (+++)‑positive for protein in her late pregnancy

**Authors:** Elisabeth Fabian, Gert Mayer, Kathrin Eller, Marion Pollheimer, Robert Queissner, Guenter J. Krejs

PMC · DOI: 10.1007/s00508-023-02316-y · Wiener Klinische Wochenschrift · 2024-02-20

## Full-text entities

- **Genes:** THSD7A (thrombospondin type 1 domain containing 7A) [NCBI Gene 221981], CRP (C-reactive protein) [NCBI Gene 1401] {aka PTX1}, TF (transferrin) [NCBI Gene 7018] {aka HEL-S-71p, PRO1557, PRO2086, TFQTL1}, ALB (albumin) [NCBI Gene 213] {aka FDAHT, HSA, PRO0883, PRO0903, PRO1341}, MPO (myeloperoxidase) [NCBI Gene 4353], HLA-G (major histocompatibility complex, class I, G) [NCBI Gene 3135] {aka MHC-G}, TG (thyroglobulin) [NCBI Gene 7038] {aka AITD3, TGN}, F5 (coagulation factor V) [NCBI Gene 2153] {aka FVL, PCCF, RPRGL1, THPH2, fV}, PRTN3 (proteinase 3) [NCBI Gene 5657] {aka ACPA, AGP7, C-ANCA, CANCA, MBN, MBT}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}
- **Diseases:** radiation (MESH:D011832), eating and stress-related disorders (MESH:D001068), addiction (MESH:D019966), abscess (MESH:D000038), Factitious disease (MESH:D005162), obesity (MESH:D009765), thrombosis (MESH:D013927), nephrotic syndrome (MESH:D009404), multiple myeloma (MESH:D009101), labor (MESH:D048949), Proteinuria (MESH:D011507), stenosis of the thoracic duct (MESH:D003251), thromboembolism (MESH:D013923), renal vein thrombosis (MESH:D012170), psychiatric (MESH:D001523), HELLP (MESH:D017359), echinococcosis (MESH:D004443), acute kidney disease (MESH:D058186), focal segmental glomerulosclerosis (MESH:D005923), bleeding (MESH:D006470), lupus antibodies (MESH:D008180), membranous lupus nephritis (MESH:D008181), watery diarrhea (MESH:D003969), coagulopathy (MESH:D001778), hypoaldosteronism (MESH:D006994), personality disorders (MESH:D010554), edema (MESH:D004487), Munchausen (MESH:D009110), nephritis (MESH:D009393), hyperthyroidism (MESH:D006980), hematuria (MESH:D006417), antiphospholipid syndrome (MESH:D016736), albuminuria (MESH:D000419), trauma (MESH:D014947), preeclampsia (MESH:D011225), end-organ dysfunction (MESH:D009102), congenital atransferrinemia (MESH:C538259), thrombocytopenia (MESH:D013921), lymphatic malformation (MESH:D008209), syndrome (MESH:D013577), diabetic nephropathy (MESH:D003928), insulinoma (MESH:D007340), infection (MESH:D007239), congenital abnormalities (MESH:D000013), hymenolepiasis (MESH:D006925), malignancy (MESH:D009369), diarrhea (MESH:D003967), hyperkalemia (MESH:D006947), depression (MESH:D003866), immune thrombocytopenia (MESH:D016553), glomerular diseases (MESH:D007674), protein loss (MESH:D011488), somatoform disorders (MESH:D013001), malaria (MESH:D008288), hypertension (MESH:D006973), pain (MESH:D010146), hypoglycemia (MESH:D007003), hematoma (MESH:D006406)
- **Chemicals:** repaglinide (MESH:C072379), AT2 blocker (-), acetylsalicylic acid (MESH:D001241), urapidil (MESH:C015568), nateglinide (MESH:D000077715), eltrombopag (MESH:C520809), magnesium sulfate (MESH:D008278), calcium (MESH:D002118), KCl (MESH:D011189), uric acid (MESH:D014527), sodium (MESH:D012964), polyacrylamide (MESH:C016679), rituximab (MESH:D000069283), urea (MESH:D014508), ketones (MESH:D007659), SDS (MESH:D012967), warfarin (MESH:D014859), heparin (MESH:D006493), glucose (MESH:D005947), bilirubin (MESH:D001663), radioiodine (MESH:C000614965), phosphate (MESH:D010710), creatinine (MESH:D003404), potassium (MESH:D011188), magnesium (MESH:D008274), nitrites (MESH:D009573), sulfonylureas (MESH:D013453), chloride (MESH:D002712)
- **Species:** Homo sapiens (human, species) [taxon 9606], Wuchereria bancrofti (agent of lymphatic filariasis, species) [taxon 6293]

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## References

40 references — full list in the complete paper: https://tomesphere.com/paper/PMC11078789/full.md

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Source: https://tomesphere.com/paper/PMC11078789