Cargando…

A neonate with intrauterine growth restriction and pseudo‐Bartter syndrome due to severe maternal eating disorder: A case report

Maternal diet before and during pregnancy plays an important role for the developing fetus. Any eating disorder in this period can cause transient or/and permanent negative effects on the mother and her offspring.

Detalles Bibliográficos
Autores principales:	Babatseva, Evgeniya, Chatziioannidis, Ilias, Tagaraki, Alexia ‐ Angeliki, Tramma, Despoina, Dampala, Kalliopi, Chatzitoliou, Efthymia, Papacharalambous, Efthymia, Mitsiakos, Georgios, Tsakalidis, Christos, Karagianni, Paraskevi, Lithoxopoulou, Maria, Anastasiadis, Kleanthis, Soubasi, Vasiliki
Formato:	Online Artículo Texto
Lenguaje:	English
Publicado:	John Wiley and Sons Inc. 2020
Materias:	Case Reports
Acceso en línea:	https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7752547/ https://www.ncbi.nlm.nih.gov/pubmed/33363775 http://dx.doi.org/10.1002/ccr3.3223

Ejemplares similares

Netherton Syndrome in a Neonate with Possible Growth Hormone Deficiency and Transient Hyperaldosteronism
por: Ilias, Chatziioannidis, et al.
Publicado: (2015)

Corrigendum to “Netherton Syndrome in a Neonate with Possible Growth Hormone Deficiency and Transient Hyperaldosteronism”
por: Chatziioannidis, Ilias, et al.
Publicado: (2015)

A New ABCA3 Gene Mutation c.3445G>A (p.Asp1149Asn) as a Causative Agent of Newborn Lethal Respiratory Distress Syndrome
por: Mitsiakos, Georgios, et al.
Publicado: (2019)

Maternal diabetes and the role of neonatal reticulocyte hemoglobin content as a biomarker of iron status in the perinatal period
por: Babacheva, Evgeniya, et al.
Publicado: (2022)

Laparoscopic evaluation and management of isolated gastric rupture in a boy after blunt abdominal injury
por: Kleanthis, Anastasiadis, et al.
Publicado: (2017)

Intercostal leiomyoma in a child: review of the literature
por: Anastasiadis, Kleanthis, et al.
Publicado: (2017)

G6PD Deficiency and Harilaou Variant in a Newborn: Intrauterine Haemolysis and Meconium Aspiration Syndrome
por: Athanasiadou, Kleoniki I., et al.
Publicado: (2021)

Repair of Postoperative Abdominal Hernia in a Child with Congenital Omphalocele Using Porcine Dermal Matrix
por: Lambropoulos, V., et al.
Publicado: (2016)

Differential diagnosis of perinatal Bartter, Bartter and Gitelman syndromes
por: Bamgbola, Oluwatoyin Fatai, et al.
Publicado: (2021)

Differential diagnosis of perinatal Bartter, Bartter and Gitelman syndromes
por: Bamgbola, Oluwatoyin Fatai, et al.
Publicado: (2020)

Neurodevelopmental Outcome in Extremely Low Birth Weight Infants at 2–3 Years of Age
por: Kyriakidou, Maria, et al.
Publicado: (2020)

Prevalence, causes and mental health impact of workplace bullying in the Neonatal Intensive Care Unit environment
por: Chatziioannidis, Ilias, et al.
Publicado: (2018)

Increased ICP as the First Sign of Pediatric-Onset Multiple Sclerosis: A Case Report and Brief Review of the Literature
por: Nikolaos, Gkiourtzis, et al.
Publicado: (2022)

A neonate with late-onset hypocalcemia due to unrecognized maternal hyperparathyroidism and a systematic overview of similar cases
por: Mitsiakos, Georgios, et al.
Publicado: (2021)

Neonatal Sepsis and Hemostasis
por: Gialamprinou, Dimitra, et al.
Publicado: (2022)

Cystinosis Presenting with Findings of Bartter Syndrome
por: Özkan, Behzat, et al.
Publicado: (2011)

Antenatal Bartter Syndrome: A Review
por: Bhat, Y. Ramesh, et al.
Publicado: (2012)

Anaesthesia for laparoscopic cholecystectomy in Bartter’s syndrome
por: Bhaskar, Bala S, et al.
Publicado: (2010)

Antenatal Bartter's syndrome with sensorineural deafness
por: Bhamkar, R. P., et al.
Publicado: (2009)

Bartter's syndrome in a geriatric patient
por: Kumar, A. C. V., et al.
Publicado: (2016)

Bartter syndrome: causes, diagnosis, and treatment
por: Cunha, Tamara da Silva, et al.
Publicado: (2018)

Association of Amelogenesis Imperfecta and Bartter's Syndrome
por: Kumar, A. C. V., et al.
Publicado: (2017)

Bartter and Gitelman syndromes: Questions of class
por: Besouw, Martine T. P., et al.
Publicado: (2019)

Childhood Bartter’s syndrome: An Indian case series
por: Sampathkumar, K., et al.
Publicado: (2010)

Nephrocalcinosis and Placental Findings in Neonatal Bartter Syndrome
por: Maruyama, Hidehiko, et al.
Publicado: (2012)

A Case of Adult-Onset Bartter’s Syndrome
por: Park, Jong Wook, et al.
Publicado: (1995)

Acquired Bartter syndrome following gentamicin therapy
por: Singh, J., et al.
Publicado: (2016)

Clinical and diagnostic features of Bartter and Gitelman syndromes
por: Walsh, Patrick R, et al.
Publicado: (2018)

Late-onset Bartter syndrome type II
por: Gollasch, Benjamin, et al.
Publicado: (2017)

Mutation spectrum of Chinese patients with Bartter syndrome
por: Han, Yue, et al.
Publicado: (2017)

Pseudo‐Bartter syndrome in children with cystic fibrosis
por: Faraji‐Goodarzi, Mojgan
Publicado: (2019)

Bartter Syndrome: Perspectives of a Pediatric Nephrologist
por: Choi, Naye, et al.
Publicado: (2022)

Replacement of the Double Meropenem Disc Test with a Lateral Flow Assay for the Detection of Carbapenemase-Producing Enterobacterales and Pseudomonas aeruginosa in Clinical Laboratory Practice
por: Tychala, Areti, et al.
Publicado: (2023)

Probable Three-Species In Vivo Transfer of bla(NDM-1) in a Single Patient in Greece: Occurrence of NDM-1-Producing Klebsiella pneumoniae, Proteus mirabilis, and Morganella morganii
por: Meletis, Georgios, et al.
Publicado: (2023)

Delayed percutaneous coronary intervention for an extensive iatrogenic left main coronary artery dissection: a case report
por: Varlamos, Charalampos, et al.
Publicado: (2022)

Bartter syndrome and cholelithiasis in an infant: is this a mere coincidence?
por: Robitaille, Pierre, et al.
Publicado: (2007)

Status epilepticus as the only presentation of the neonatal Bartter syndrome
por: Patra, Soumya, et al.
Publicado: (2012)

Renal transplantation in a patient with Bartter syndrome and glomerulosclerosis
por: Lee, Se Eun, et al.
Publicado: (2011)

Congenital chloride diarrhea misdiagnosed as pseudo-Bartter syndrome
por: Saneian, Hossein, et al.
Publicado: (2013)

Adult presentation of Bartter syndrome type IV with erythrocytosis
por: Heilberg, Ita Pfeferman, et al.
Publicado: (2015)

Cannot write session to /tmp/vufind_sessions/sess_q409q55q12tj45qmpomuuk39ek