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All Posts By

Darlene Silverman

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Research: Laparoscopic repair of Morgagni’s hernia in an elderly female patient.

J Surg Case Rep. 2020 Jun 15;2020(6):rjaa182. doi: 10.1093/jscr/rjaa182. eCollection 2020 Jun. Laparoscopic repair of Morgagni’s hernia in an elderly female patient. Leite C1, Aveiro D1, Simão R1, Coelho S1, Casimiro C1. Author information Abstract Morgagni’s hernia is a very uncommon congenital diaphragmatic hernia. A few patients may remain asymptomatic until adulthood. Clinical presentation may include bowel obstruction, chest pain or dyspnoea. The authors report …

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Research: A proteome signature of umbilical cord serum associated with congenital diaphragmatic hernia.

Nagoya J Med Sci. 2020 May;82(2):345-354. doi: 10.18999/nagjms.82.2.345. https://pmlegacy.ncbi.nlm.nih.gov/pubmed/32581413 A proteome signature of umbilical cord serum associated with congenital diaphragmatic hernia. Tachi A1, Moriyama Y1, Tsuda H2, Miki R3, Ushida T1, Miura M1, Ito Y1, Imai K1, Nakano-Kobayashi T1, Hayakawa M4, Kikkawa F1, Kotani T1,4. Author information Abstract Congenital diaphragmatic hernia (CDH) is a congenital anomaly characterized by a defect in the diaphragm. Despite the recent improvements in its treatment, CDH …

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Research: History Matters: A 20-Month-Old Child With Cough and Congestion.

Clin Pediatr (Phila). 2019 Nov;58(13):1452-1454. doi: 10.1177/0009922819850484. Epub 2019 May 21. https://pmlegacy.ncbi.nlm.nih.gov/pubmed/31113228 History Matters: A 20-Month-Old Child With Cough and Congestion. Ellis S1, Kilaikode S1. Author information PMID: 31113228 DOI: 10.1177/0009922819850484

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Research: Acute Budd-Chiari syndrome caused by inferior vena cava compression from a congenital diaphragmatic hernia.

Ann R Coll Surg Engl. 2020 Jun 15:e1-e3. doi: 10.1308/rcsann.2020.0106. [Epub ahead of print] https://pmlegacy.ncbi.nlm.nih.gov/pubmed/32538105 Acute Budd-Chiari syndrome caused by inferior vena cava compression from a congenital diaphragmatic hernia. Wcislo KM1,2, Hall CE1,2, Abbassi-Ghadi N3. Author information Abstract Acute Budd-Chiari syndrome is a rare condition characterised by obstruction of hepatic venous outflow. We describe the case of a 52-year-old …

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Research: Late presenting congenital diaphragmatic hernia misdiagnosed as a pleural effusion: A case report.

Medicine (Baltimore). 2020 Jun 12;99(24):e20684. doi: 10.1097/MD.0000000000020684. https://pmlegacy.ncbi.nlm.nih.gov/pubmed/32541516 Late presenting congenital diaphragmatic hernia misdiagnosed as a pleural effusion: A case report. Shin HB1,2, Jeong YJ1,2. Author information Abstract RATIONALE: Late presenting congenital diaphragmatic hernia (CDH) that develops after the neonatal period has various clinical manifestations and can often be misdiagnosed as pleural effusion, pneumonia, or pneumothorax. We report an adolescent case …

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Research: Intestinal obstruction due to a bilateral Morgagni hernia.

Cir Esp. 2020 Jan;98(1):45. doi: 10.1016/j.ciresp.2019.02.009. Epub 2019 Apr 7. https://pmlegacy.ncbi.nlm.nih.gov/pubmed/30971338 Intestinal obstruction due to a bilateral Morgagni hernia. [Article in English, Spanish]Yagüe Rigopoulou N1, Alegre Torrado C2, Marcacuzco Quinto A2. Author information PMID: 30971338 DOI: 10.1016/j.ciresp.2019.02.009

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Research: Bi-allelic loss of function variants of TBX6 causes a spectrum of malformation of spine and rib including congenital scoliosis and spondylocostal dysostosis.

J Med Genet. 2019 Sep;56(9):622-628. doi: 10.1136/jmedgenet-2018-105920. Epub 2019 Apr 22. https://pmlegacy.ncbi.nlm.nih.gov/pubmed/31015262 Bi-allelic loss of function variants of TBX6 causes a spectrum of malformation of spine and rib including congenital scoliosis and spondylocostal dysostosis. Otomo N1,2, Takeda K1,2, Kawai S3,4,5, Kou I1, Guo L1, Osawa M6, Alev C3, Kawakami N7, Miyake N8, Matsumoto N8, Yasuhiko Y9, Kotani T10, Suzuki T11, Uno K11, Sudo H12, Inami S13, Taneichi H13, Shigematsu H14, Watanabe K15, Yonezawa I16, Sugawara R17, Taniguchi Y18, Minami S10, Kaneko K16, Nakamura M2, Matsumoto …

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Research: The clinical overlap between cardiac-urogenital syndrome, Meacham syndrome, and PAGOD syndrome. Report of a new patient with cardiac-urogenital syndrome.

Am J Med Genet A. 2020 Jun;182(6):1532-1534. doi: 10.1002/ajmg.a.61551. Epub 2020 Mar 17.https://pmlegacy.ncbi.nlm.nih.gov/pubmed/32181572 The clinical overlap between cardiac-urogenital syndrome, Meacham syndrome, and PAGOD syndrome. Report of a new patient with cardiac-urogenital syndrome. Alves D1, Leão M2. Author information Comment on Review of the phenotypic spectrum associated with haploinsufficiency of MYRF. [Am J Med Genet A. 2019] PMID: 32181572 DOI: 10.1002/ajmg.a.61551

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Research:Does the Presence of a Hernia Sac Improve Survival in Newborns with Congenital Diaphragmatic Hernia? A United Kingdom Single-Center Experience.

Eur J Pediatr Surg. 2020 Jun 11. doi: 10.1055/s-0040-1713131. [Epub ahead of print] https://pmlegacy.ncbi.nlm.nih.gov/pubmed/32526780 Does the Presence of a Hernia Sac Improve Survival in Newborns with Congenital Diaphragmatic Hernia? A United Kingdom Single-Center Experience. Jawaid W1, Sampat K2, Losty PD2. Author information Abstract INTRODUCTION:  A developing body of literature suggests that the presence of a hernia sac in fetuses with congenital diaphragmatic hernia (CDH) may …

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Research: Cochlear Implantation Outcomes in Children with Agenesis of the Corpus Callosum: A Retrospective Study and A Review of the Literature

J Int Adv Otol. 2019 Dec;15(3):364-367. doi: 10.5152/iao.2019.6577. Cochlear Implantation Outcomes in Children with Agenesis of the Corpus Callosum: A Retrospective Study and A Review of the Literature. Özdemir S1, Tuncer Ü1, Sürmelioğlu Ö1, Tarkan Ö1, Çelik F1, Kıroğlu M1, Dağkıran M1, Şahin P1, Tezer N1, Akar F1. Author information Abstract OBJECTIVES: The aim of the present study was to analyze the outcomes of cochlear …

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Research: Acute massive gastric dilatation: a rare, forgotten complication of fundoplication.

BMJ Case Rep. 2020 May 27;13(5). pii: e232479. doi: 10.1136/bcr-2019-232479. https://pmlegacy.ncbi.nlm.nih.gov/pubmed/32467115 Acute massive gastric dilatation: a rare, forgotten complication of fundoplication. Lau SE#1, Boam T#2,3, Parsons S4, Motiwale S3. Author information Abstract An 8-year-old boy with a history of multiple neonatal laparotomies, including congenital diaphragmatic hernia repair and an open fundoplication, presented acutely with severe abdominal pain, distension, vomiting and shock. …

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Research: Congenital diaphragmatic hernia: postnatal predictors of mortality.

Arch Argent Pediatr. 2020 Jun;118(3):173-179. doi: 10.5546/aap.2020.eng.173. https://pmlegacy.ncbi.nlm.nih.gov/pubmed/32470252 Congenital diaphragmatic hernia: postnatal predictors of mortality. [Article in English, Spanish; Abstract available in Spanish from the publisher]Salas GL1, Otaño JC2, Cannizzaro CM2, Mazzucchelli MT2, Goldsmit GS2. Author information Abstract in English, Spanish INTRODUCTION: Congenital diaphragmatic hernia (CDH) prevalence is low while its associated morbidity and mortality rates are high. Postnatal prognostic factors on the …