G Girschick

Center for Prenatal Diagnosis and Human Genetics, Kudamm-199, Berlín, Berlin, Germany

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Publications (31)50.04 Total impact

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    ABSTRACT: Significant placental insufficiency, indicated by Doppler ultrasound findings of absent or reverse end-diastolic flow velocities (AREDV), is associated with increased morbidity and mortality. Analysis of blood flow in the ductus venosus should assist in early intrauterine recognition of threatened foetuses. 58 high-risk pregnancies with umbilical AREDV were repeatedly examined (n=364). Doppler findings were correlated with neonatal signs of deterioration (ratio of normoblasts to leukocytes, pH, base excess, Apgar score), as well as short-term morbidity [need for intubation, duration of assisted respiration, evidence of respiratory distress syndrome (RDS), bronchopulmonary dysplasia (BPD), necrotising enterocolitis (NEC), intraventricular haemorrhage (IVH grade III+IV)] against the analysis of the blood flow findings (normal or increased pulsitility, absence or reverse end-diastolic flow) in the umbilical arteries (AU), the middle cerebral arteries (ACM) and ductus venosus (DV) relating these to birth weight and the duration of the pregnancy. The median period of observation was 12.8 days, 48% of the foetuses showed an abnormal ductus venosus flow and 26% an absent venous or reverse end-diastolic flow. The median date of delivery was 30 weeks, with a mean birth weight of 816 g. 93% were live births with 12% dying postnatally. Although the criteria for postnatal morbidity (BPD, NEC, IVH III+IV) and mortality did not correlate with changes in arterial and venous Doppler parameters in our group, there was a significant relationship between the normoblast count, known to be a marker of chronic hypoxia. The Apgar 10 minte score, umbilical arterial pH and base excess were correlated with changes in the DV flow curves. Healthy survival started, irrespective of arterial or venous blood flow criteria, from 27+0 weeks of pregnancy. If born between 27.0 and 30+6 weeks, the infants were more likely to be healthy the less the blood flow had been compromised. A birth weight of 590 g (sensitivity 62.5%; specificity 93.5%) and gestational age of 28+5 weeks (sensitivity 87.5%; specificity 90.3%) were shown to be cut-off points between healthy survival and survival with serious neonatal complications. © Georg Thieme Verlag KG Stuttgart · New York.
    Zeitschrift für Geburtshilfe und Neonatologie 02/2015; 219(1):28-36. DOI:10.1055/s-0034-1394387 · 0.48 Impact Factor
  • I Frauenschuh · G Girschick · S Blissing · M Rehn · J Dietl · T Müller
    Geburtshilfe und Frauenheilkunde 07/2012; 72(07). DOI:10.1055/s-0032-1318567 · 0.94 Impact Factor
  • I. Frauenschuh · G. Girschick · S. Blissing · M. Rehn · J. Dietl · T. Mueller
    Geburtshilfe und Frauenheilkunde 07/2012; 72(7):P46-P46. · 0.94 Impact Factor
  • U Zollner · M Rehn · G Girschick · J Dietl
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    ABSTRACT: Malformations of the central nervous system are among the most frequent congenital anomalies. At best, a qualified and standardised screening of the foetal brain is possible between the 18th and the 22nd week. The newly decided modification of the maternity directives envisages an extended screening upon request. This extended screening refers to the central nervous system and the representation of the ventricles, the evaluation of the head shape and the cerebellum and the back. The examination of the foetal brain should be carried out in a structured way. Three axial planes, the transventricular, the transthalamic and the transcerebellar planes, suffice to represent and measure all structures which are of importance for the screening. In case of ventricular anomalies, anomalies of the head shape, anomalies of the cerebellum and irregularities of the dorsal skin outlined in the second screening a further diagnostic procedure should be initiated. This diagnostic work-up should include a detailed neurosonography, a diagnostic evaluation of the organs and eventually further examination in the form of a caryotyping, determination of the infectology or a foetal MRI. The present article offers an overview of possible CNS abnormalities which could be recognised during the second screening according to the extended maternity directives and describes which differential diagnostics should be considered. In detail, anomalies of the head size (microcephaly, macrocephaly), of the head size (brachycephaly, dolichocephaly, cavities of the cranium, banana sign, etc.,), ventricular abnormalities, anomalies of the cerebellum (cerebellum hypoplasia, abnormal cerebellum shape) and abnormalities of the intermediate line and the intracerebral space requirements are discussed.
    Zeitschrift für Geburtshilfe und Neonatologie 02/2012; 216(1):1-10. DOI:10.1055/s-0031-1299770 · 0.48 Impact Factor
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    ABSTRACT: Junctional epidermolysis bullosa with pyloric atresia (JEB-PA) is a rare autosomal recessive disease with blister formation within the lamina lucida due to mutations in the integrin β4 (ITGB4) and α6 (ITGA6) genes. A female preterm infant, first child of healthy non-consanguineous parents, was born at 26 + 4 weeks of gestation by caesarean section, following polyhydramnion and abruption of placenta. She presented with extensive areas of denuded skin on both lateral sides of the head, neck and extremities. Auricles were hypoplastic. Abdominal ultrasound and X-ray were suggestive of pyloric atresia which was revised surgically on the 4th day of life. Further course was complicated by progressive skin detachment, sepsis, and renal insufficiency with fatal outcome at 18 days of age. Immunofluorescence mapping of cryopreserved skin showed junctional cleft formation with negative staining for integrin α6 and integrin β4. Mutational analysis disclosed compound heterozygosity for two novel nonsense mutations in the ITGB4 gene: c.600dupC/p.F201fsX14 and c.2533C>T/p.Q845X. 2 subsequent pregnancies were terminated following prenatal diagnosis disclosing the same ITGB4 mutations, a 4th pregnancy was unaffected. We describe a case of lethal JEB-PA with negative immunoreactivity to integrin α6 and integrin β4 predicting a poor outcome. Identification of compound heterozygosity for two novel ITGB4 mutations in the affected preterm infant permitted prenatal diagnosis and finally birth of a healthy sibling.
    Klinische Pädiatrie 01/2012; 224(1):8-11. DOI:10.1055/s-0031-1285877 · 1.06 Impact Factor
  • U Zollner · M Rehn · G Girschick · J Dietl
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    ABSTRACT: Intrauterine growth restriction (IGUR) can have different etiologies, but placental insufficiency is the clinically most relevant. Fetuses with IUGR have a significantly higher morbidity and mortality than normally grown fetuses of the same gestational age. It is important to distinguish a growth restricted fetus from a normal, small fetus and from a fetus being small because of a disease, e.g., an aneuploidy. This differentiation requires the knowledge of the gestational age and the use of multiple imaging modalities. Serial assessments of fetal growth by ultrasound are necessary to recognize declining growth. Doppler sonography can detect changes in the uteroplacentar and the fetal perfusion. Blood vessels of clinical relevance are the uterine arteries, the umbilical artery, the middle cerebral artery and the ductus venosus. When no fetal anomalies can be detected, fetal growth is parallel to the percentiles and Doppler sonography measurements are normal, IUGR is unlikely. In most IUGR fetuses, a typical sequence of circulatory changes and ultrasound findings can be observed. As there is no evidence-based treatment option for IUGR until now, obstetric management consists in defining the optimal time of delivery. This means weighing the risks of prematurity against the risks of a potentially hostile intrauterine environment.
    Zeitschrift für Geburtshilfe und Neonatologie 04/2011; 215(2):49-59. DOI:10.1055/s-0030-1255023 · 0.48 Impact Factor
  • Source
    U Zollner · K Balling · G Girschick · A Mastorakis · D Klotz · M Rehn
    Ultrasound in Obstetrics and Gynecology 10/2010; 36(S1):298. DOI:10.1002/uog.8767 · 3.85 Impact Factor
  • Source
    M Rehn · G Girschick · U Zollner · T Deuchert · E Marques-Maggio · J Dietl
    Ultrasound in Obstetrics and Gynecology 09/2009; 34(S1):233. DOI:10.1002/uog.7203 · 3.85 Impact Factor
  • MB Wamsler · U Zollner · R Wössner · M Rehn · J Dietl · G Girschick
    Ultraschall in der Medizin 09/2009; 30. DOI:10.1055/s-0029-1239726 · 4.92 Impact Factor
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    ABSTRACT: Hypophosphatasia (HP) is an inborn error of bone metabolism transmitted predominantly as an autosomal-recessive trait. It is characterized by a reduced activity of the tissue-nonspecific isoenzyme of alkaline phosphatase (TNSAP) and elevated concentrations of its substrates, including pyrophosphates. Clinical symptoms include defective bone mineralisation with bone deformities, fractures and as recently defined chronic non-bacterial osteomyelitis. Renal damage due to calcification, craniosynostosis and dental abnormalities with premature loss of dentition are further symptoms, which have been described as characteristic in the ESPED inquiry of 2004. Knowledge about the mechanisms underlying cell activation leading to inflammation and tissue destruction is still limited in HP. Recent investigations have provided evidence that calcium pyrophosphate crystals are essentially involved in activating inflammatory signal transduction pathways via different receptors of the innate immune system. Laboratory assays, genetic counselling and testing, and radiologic imaging can confirm the diagnosis. Because symptoms are highly variable in their clinical expression, patients should be followed by a HP-experienced multidisciplinary team (paediatrician, radiologist, orthopedist, neurosurgeon, dentist). At the moment symptomatic support and treatment is most important because a causative therapy, e. g. enzyme replacement therapy, is not yet available.
    Klinische Pädiatrie 07/2009; 221(4):219-26. DOI:10.1055/s-0029-1220718 · 1.06 Impact Factor
  • U Zollner · E Klopocki · M Rehn · E Kunstmann · G Girschick · J Dietl
    Zeitschrift für Geburtshilfe und Neonatologie 04/2009; 213. DOI:10.1055/s-0029-1222890 · 0.48 Impact Factor
  • M Rehn · W Schmitt · R Mai · E Frieauff · J Dietl · G Girschick
    Zeitschrift für Geburtshilfe und Neonatologie 04/2009; 213. DOI:10.1055/s-0029-1222887 · 0.48 Impact Factor
  • G Girschick · U Zollner · J Wirbelauer · M Rehn · J Dietl
    Zeitschrift für Geburtshilfe und Neonatologie 04/2009; 213. DOI:10.1055/s-0029-1222760 · 0.48 Impact Factor
  • P Richl · H Morbach · U Stern · G Girschick · P Lipsky · HJ Girschick
    Zeitschrift für Geburtshilfe und Neonatologie 04/2009; 213. DOI:10.1055/s-0029-1222849 · 0.48 Impact Factor
  • MB Wamsler · G Girschick · A Zettl · J Dietl · M Rehn
    Geburtshilfe und Frauenheilkunde 09/2008; 68(S 01). DOI:10.1055/s-0028-1088963 · 0.94 Impact Factor
  • G Girschick · M Rehn · J Krauß · J Wirbelauer · M Stenzel
    Geburtshilfe und Frauenheilkunde 09/2008; 68(S 01). DOI:10.1055/s-0028-1089267 · 0.94 Impact Factor
  • AK Morr · M Rehn · U Völker · J Dietl · G Girschick
    Geburtshilfe und Frauenheilkunde 09/2008; 68(S 01). DOI:10.1055/s-0028-1089121 · 0.94 Impact Factor
  • M Wamsler · M Rehn · L Rieger · J Dietl · G Girschick
    Ultraschall in der Medizin 08/2008; 29. DOI:10.1055/s-0028-1085851 · 4.92 Impact Factor
  • S Blissing · R Roloff · G Girschick · T Frambach · J Dietl
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    ABSTRACT: The prevalence of overweight and obesity in pregnant women has increased during the last decades (in our examination period from 10.9 to 29.8 %). Maternal obesity is a risk factor for pregnancy, delivery and the newborn. Does the neonatal outcome of pregnancies with maternal overweight and obesity in 2005 differ from that in 1980? All patients with a body mass index (BMI) > 25 kg / m (2) who delivered in 1980 (n = 130) and in 2005 (n = 392) at the University Hospital Würzburg were evaluated retrospectively. The neonatal result of singletons born at term was studied (1980: n = 125; 2005: n = 315). The rates of macrosomia > 4500 g (5.6 vs. 1.3 %) and shoulder dystocia (4.8 vs. 0.3 %) declined significantly. No significant differences were found regarding the mean newborn weight (3560 vs. 3508 g), weight percentile (55.5 vs. 56.4 %), length (51 cm), head size (35 cm), fetal distress (3.2 vs. 3.8 %), respiratory insufficiency (3.2 vs. 2.2 %), 5-min-Apgar (9.77 vs. 9.69) and arterial umbilical cord pH (7.27 vs. 7.26). Birth weight was not associated with the degree of obesity in 2005 compared to 1980. Despite the increasing prevalence and severity of obesity in pregnant women most parameters of neonatal outcome did not change. The observed relative rate of macrosomia and shoulder dystocia declined, but the case number of these complications is still relevant. Obviously obstetricians have responded appropriately to the changing risk profile.
    Zeitschrift für Geburtshilfe und Neonatologie 06/2008; 212(3):94-9. DOI:10.1055/s-2008-1004803 · 0.48 Impact Factor
  • JB Engel · M Rehn · J Wirbelauer · J Dietl · G Girschick
    Geburtshilfe und Frauenheilkunde 05/2008; 68(05). DOI:10.1055/s-2008-1079158 · 0.94 Impact Factor

Publication Stats

48 Citations
50.04 Total Impact Points


  • 2010
    • Center for Prenatal Diagnosis and Human Genetics, Kudamm-199
      Berlín, Berlin, Germany
  • 2001–2009
    • University of Wuerzburg
      • Department of Obstetrics and Gynaecology
      Würzburg, Bavaria, Germany