Surasak Puvabanditsin, MD

1. Puvabanditsin S, Shim M, Suell J, Manzano J, Blackledge K, Bursky-Tammam A, Mehta R. Prune Belly Syndrome associated with interstitial 17q12 microdeletion. Case Rep Urol. 2022 Feb 14;2022:7364286. doi: 10.1155/2022/7364286. eCollection 2022.PMID: 35198258 2. Puvabanditsin S, Kased R, Maskey A, Mehta R, Murphy S. Neonatal hemophilia A. Consultant. Published online May 21, 2021. doi:10.25270/con.2021.05.00006 3. Puvabanditsin S, Maskey A, Kased R, Haleem S, Mehta R. Spinal dysraphism, club feet, and dextrocardia with situs inversus totalis in a neonate: a rare association and review. Case Rep. Perinat. Med. 2020; 9(1): 20200061. DOI: https://doi.org/10.1515/crpm-2020-0061 4. Puthenpura V, Gueye-Ndiaye S, Joshi S, Puvabanditsin S, Carayannopoulos MO. Social and Legal Implications of Urine Drug Screen Analysis in the Neonate: A Case of Suspected Specimen Mishandling.Clin Chim Acta. 2020 Sep 28:S0009-8981(20)30464-2. PMID 33002470 5. Puvabanditsin S, Negroponte E, Jang P, Hedges A, Kased R, Mehta R. Multiple Congenital Anomalies in a Patient with Interstitial 6q26 Deletion. Mol Syndromol. 2020 Jan;10(5):276-280. doi: 10.1159/000503698. PMID: 32021599 6. Puvabanditsin S, Jacob M, Jalil M, Bhattarai S, Patel Q, Sadiq M, Mehta R. Extended-Spectrum Beta-Lactamase-Producing Escherichia coli Meningitis and Cerebral Abscess in a Neonate: Therapeutic Challenge. Case Rep Infect Dis. 2019 Mar 28;2019: 6874192. PMID 31032129 7. Puvabanditsin S, Gengel N, Botti C, Jacob M, Jalil M, Cabrera K, Mehta R. 8p 11 Microduplication Is Associated with Neonatal Stridor. Mol Syndromol. 2019 Jan;9(6):324-327. PMID: 30800050 8. Puvabanditsin S, Sadiq M, Jacob M, Jalil M, Cabrera K, Choudry O, Mehta R. 11p15.4 Microdeletion Associates with Hemihypertrophy. Case Rep Genet. 2018 Oct 30;2018:2746347. PMID: 30510815 9. Puvabanditsin S, Botwinick M, Chen CW, Joshi A, Mehta R. Biliary Tract Abnormalities as a Cause of Distal Bowel Gas in Neonatal Duodenal Atresia. Case Rep Surg. 2018 Jun 26;2018:8041427. doi: 10.1155/2018/8041427. PMID: 30046504 10. Puvabanditsin S, February M, Mayne J, McConnell J, Mehta R. Cleidocranial Dysplasia With 6p21.1-p12.3 Microdeletion: A Case Report and Literature Review. Cleft Palate Craniofac J. 2018 Jul;55(6):891-894. doi: 10.1597/15-306. PMID: 27500518 11. Puvabanditsin S, Chen CW, Botwinick M, Hussein K, Mariduena J, Mehta R. Ventriculomegaly and cerebellar hypoplasia in a neonate with interstitial 11q 24 deletion in Jacobsen syndrome region. Clin Case Rep. 2018 May 22;6(7):1268-1275. doi: 10.1002/ccr3.1560 PMID: 29988670 12. Puvabanditsin S, Puthenpura V, Gueye-Ndiaye S, Takyi M, Madubuko A, Walzer L, Mehta R. Congenital second-degree heart block and total anomalous pulmonary venous return associated with microduplication of 1q32.2. Ann Pediatr Cardiol. 2018 May-Aug;11(2):194-196. doi: 10.4103/apc.APC_21_17. PMID: 29922018 13. Puvabanditsin S, Burger R, Puthenpura V, Walzer L, Madubuko A, Minerowicz C, Mehta R. A Giant Gastroschisis Associated with Pulmonary Hypoplasia and Spinal Anomaly: A Case Report and a Literature Review. Case Rep Pathol. 2018 May 2;2018:8378769. doi: 10.1155/2018/8378769 PMID: 29854529 14. Puvabanditsin S, Abellar R, Madubuko A, Mehta R, Walzer L. Pulmonary Vasculitis and a Horseshoe Kidney in Noonan Syndrome. Case Rep Pathol. 2018 Jan 29;2018:6829586. doi: 10.1155/2018/6829586. PMID: 29670795 15. Puvabanditsin S, Chen CW, Vinod S, Mehta MS, Choudry O, Walzer L. Bile-stained amniotic fluid: a case report. J Med Case Rep. 2017 Sep 6;11(1):254. doi: 10.1186/s13256-017-1419-8. PMID: 28874174 16. Puvabanditsin S, Zaldana F, Raviola J, Suell J, Hussein K, Walzer L, Mehta R. Vessel Perforation and False Tracking Resulting from Umbilical Artery Catheterization: A Case Report and Literature Review. Pediatr Dev Pathol. 2017 Sep-Oct;20(5):426-431. PMID: 28812467 17. Puvabanditsin S, Mehta R, Palomares K, Gengel N, Da Silva CF, Roychowdhury S, Gupta G, Kashyap A, Sorrentino D. Vein of Galen malformation in a neonate: A case report and review of endovascular management. World J Clin Pediatr. 2017 Feb 8;6(1):103-109. PMID: 28224101 18. Puvabanditsin S, Gurp JV, February M, Marwa K, Mayne J, McConnell JA, Mehta R. VACTERL association and caudal regression with Xq25-q27.3 microdeletion: a case report. Fetal Pediatr Pathol. 2016;35(2):133-41. doi: 10.3109/15513815.2016.1139019. PMID: 26881326 19. Puvabanditsin S, Gueye S, Puthenpura V, Gengel N, Tam V, Mehta R. Microduplication of 17p[dup(17)(12p11.2)]: report of a neonate with a spina bifida and cardiac anomalies and a literature review. Genet Couns. 2016; 27(4): 503-507. PMID: 30226970 20. Puvabanditsin S, February M, Stefano VD, Vinod S, Minerowicz C, Hussein K, Mayne J, Mehta R. Osteocraniosplenic syndrome–hypomineralized skull with gracile long bones and splenic hypoplasia: a case report and literature review. Genetic Couns. 2016;. 27(2): 149-157. PMID: 29485259 21. Puvabanditsin S, Gengel NK, February M, Mayne J, Mehta R. Partial trisomy 4p and partial monosomy 13q: case report and a literature review. Genet Couns. 2016;27(1):35-41. PMID: 27192890 22. Puvabanditsin S, Garrow E, February M, Yen E, Mehta R. Esophageal atresia with recurrent tracheoesophageal fistulas and microduplication 22q11.23. Genet Couns. 2015;26(3):313-20. PMID: 26625662 23. Puvabanditsin S, February M, Garrow E, Bruno C, Mehta R. Our experience with a severe case of aplasia cutis congenita with a large skull defect. Int J Dermatol. 2016 Oct;55(10):1151-3. doi: 10.1111/ijd.13008. PMID: 26228315 24. Puvabanditsin S, February M, Shaik T, Kashyap A, Bruno C, Mehta R. 2q31.1 microdeletion syndrome: case report and literature review. Clin Case Rep. 2015 Jun;3(6):357-60. PMID: 26185628 25. Puvabanditsin S, February M, Francois L, Garrow E, Bruno C, Mehta R. 7q21.11 Microdeletion in a Neonate With Goldenhar Syndrome: Case Report and a Literature Review. Cleft Palate Craniofac J. 2016 Mar;53(2):249-52. doi: 10.1597/14-308. PMID: 26068384 26. Puvabanditsin, S., Malik, I., Garrow, E., Francois, L, Mehta, R. Clival encephalocele and 5q15 deletion: A case report. J Child Neurol. 2015 ;30:505-8. PMID: 24762864 27. Puvabanditsin S, Memon N, Chekmareva M, Di Stefano V, Mehta R. Cloves syndrome: a case report and perinatal diagnostic findings. Genet Couns. 2014;25:265-70. PMID: 25365848 28. Puvabanditsin S, Malik I, Weidner LM, Jadhav S, Sanderman J, Mehta R. Neonatal umbilical cord myiasis in New Jersey. J Perinatol. 2014;34:718-9. PMID: 25179383 29. Khan I, Rizvi SA, Malik I, Weinberger, B, Puvabanditsin S, Hegyi T. Extravasation of Intravenous Fluid in a Preterm Neonate. Consultant for Pediatricians. 2014;12(4):133-135. 30. Puvabanditsin, S., Garrow, E., Balbin, J., Quan, M., Mehta, R. Congenital lumbar hernia associated with lumbocostovertebral syndrome. Consultant for Pediatricians 2014;13:71-73. 31. Puvabanditsin S, Khan I, Torres S, Mahadeo AM, Garrow E. Female Genital Trauma Associated With Breech Presentation. Consultant for Pediatricians 2013;12(11):516-517. http://www.pediatricsconsultant360.com/article/female-genital-trauma-associated-breeh-presentation 32. Malik I, Puvabanditsin S, Memon N, Khan I, Stahl GE. Use of a Fogarty balloon catheter to decompress pneumatocele in preterm neonates. OA Case Reports 2013 Dec 24;2(15):148. 33. Puvabanditsin, S., Khan, I., Torres, S., Mahadeo, A.M., Garrow, E., Female genital trauma associated with breech presentation. Consultant for Pediatricians 2013;12:516-517. 34. Puvabanditsin, S.,Di Stefano, V.,Garrow, E.,Wong, R.,Eng, J.,Balbin, J. Ectopia cordis; Hong Kong Med J. 2013;19(5):447-450. PMID 2408858. 35. Puvabanditsin, S.,Khan, I.,Garrow, E.,Botti, C.,Lambert, G.,Quan, M. Partial trisomy 15q23 and partial monosomy 5p15.32: Case report and a literature review.; Am. J. Med. Genet. A. 2013;161: 3201-3204. PMID: 23610861 36. Puvabanditsin, S.,Memon, N.,Lambert, G.,Cross, G.,El-Khawam, R.,Botti, C.,Balbin, J. Partial trisomy 3p24.3 and partial monosomy 5p15.33: case report and a literature review. Genet. Couns. 2013;24(1)13-20. PMID: 24038903 37. Puvabanditsin S, Memon N, Do MT, Malik I, Lambert G, Balbin J. Superior vena cava syndrome causing chylothoraces in a preterm neonate: a case report and literature review. Case Rep Perinat Med 2013;2: 75–79. 38. Puvabanditsin S, Garrow E, Gowda S, Joshi-Kale M, Mehta R. A gelatinous human tail with lipomyelocele: case report. J Child Neurol. 2013;28:124-127. PMID: 22467742. 39. Chassaing N, Sorrentino S, Davis EE, Martin-Coignard D, Iacovelli A, Paznekas W, Webb BD, Faye-Petersen O, Encha-Razavi F, Lequeux L, Vigouroux A, Yesilyurt A, Boyadjiev SA, Kayserili H, Loget P, Carles D, Sergi C, Puvabanditsin S, Chen CP, Etchevers HC, Katsanis N, Mercer CL, Calvas P, Jabs EW. OTX2 mutations contribute to the otocephaly-dysgnathia complex. J Med Genet. 2012;49:373-379. PMID: 22577225 40. Puvabanditsin S, Garrow E, Lambert G, Botti C, Gowda S, Kathiravan S, Brooks SS. Partial trisomy 10p12.33 and partial monosomy 13q32.1: case report and a literature review. Genet Couns 2011;22:263-272. PMID:222029167 41. Puvabanditsin S, Savla J, Garrow E, Kierson ME, Rosenbaum RD, Brandsma E . Symmetrical upper limb peromelia and lower limb amelia associated with persistent omphalomesenteric duct: a case report. Clin Dysmorphol. 2011;20:102-6. PMID: 21278573 42. Puvabanditsin S, Nagar MS, Eugene G, Mayoor B, Joshi M. Four-vessel umbilical cord associated with multiple congenital anomalies: a case report and literature review. Fetal Pediatr Pathol. 2011;30:98-105. PMID: 21391749. 43. Puvabanditsin S, Nagar MS, Joshi M, Lambert G, Garrow, Brandsma E. Microdeletion of 16p11.2 associated with Endocardial Fibroelastosis. Am J Med Genet Part A 2010;152A:2383–2386. PMID: 20683992 44. Puvabanditsin, S, Eugene G, Weerasethsiri, R, Joshi, M, Brandsma, E. Nicolau’s syndrome induced by intramuscular vitamin K injection in an extremely low birth weight newborn. Int J Dermatol. 2010;49:1047-1049. PMID: 20883268 45. Puvabanditsin S, Garrow E, Savla J, Brandsma E, Kunjumon B, Gadi I. Partial trisomy 19p13.3 and partial monosomy 1p36.3 case report and a literature review. Am J Med Genet A. 2009;149A:1782-5. PMID: 19610110 46. Puvabanditsin S, Garrow E, Chinnakaruppan N, Bhatt M, Brandsma E. Calcified meconium balls in a newborn: an unusual case with imperforate anus, rectourinary fistula, colpocephaly, and agenesis of corpus callosum. Pediatr Surg Int. 2009;25:441-3 PMID: 19319541 47. Puvabanditsin S, Garrow E, Weerasethsiri R, Davis SE, Patel N, Azuma MA. Fracture of a Broviac catheter in a low birth weight infant. Hong Kong Med J 2008;14(5):411-413 PMID: 18840917 48. Puvabanditsin S, Garrow E, Patel N, D’Elia A, Zaafran A, Phattraprayoon N, Davis SE Choroid plexus hyperplasia and Monosomy 1p36: report of new findings. J Child Neurology 2008;23(8):922-925. PMID: 18660475 49. Puvabanditsin S, Dumitrescu C, Garrow E, Elnahar Y, Ladie DE, Phattraprayoon . Not a Dandy Walker malformation but congenital cytomegalovirus infection. HK J Paediatr. 2008;13:56-59. 50. Puvabanditsin S, Garrow E, Razi S, Mohar AG, Tadros JJ, Phattraprayoon N, Patel P. A Y/15 translocation in a 45,X male with Prader-Willi syndrome. Genet Couns 2007;18:417-421 PMID: 18286823 51. Puvabanditsin S, Zaafran A, Diwan R, Garrow E, Mehta D, Phattraprayoon N. Bacillus cereus meningoencephalitis in a neonate. HK J Paediatr. 2007;12:293-296. 52. Puvabanditsin S, Garrow E, Turcanu DS, Umaru S, Mohar AG, Mehta D. Tetralogy of Fallot, total anomalous Pulmonary venous return, and complete arterioventricular septal defects: a rare association. Chirurgia 2007;20: 35-38. 53. Puvabanditsin S, Garrow E, Razi S, Davis E, Padilla J, Chowdawarapu SC. Cardiac tamponade as fatal complication of a percutaneous central venous line in a preterm neonate. Chirurgia 2006;19:435-438. 54. Puvabanditsin S, Garrow E, Snider ZG, Azuma MA, Tavaria A, Cerefice M. Dandy-Walker malformation in mosaic Klinefelter syndrome. Genet Couns. 2006;17:245-248. PMID: 16970044 55. Puvabanditsin S, Garrow E, Umaru S, Padilla J, Chowdawarapu S, Biswas A. Otocephaly and pulmonary malformation association: two case reports. Genet Counsel. 2006;17:167-171. PMID: 16970034 56. Puvabanditsin S, Garrow E, Titapiwatanakun R, Getachew R, Patel JB. Severe calcinosis in an infant. Pediatr Radiol. 2005;35(5):539-542. PMID: 15565339 57. Puvabanditsin S,Garrow E, Augustin G, Titapiwatanakul R, Kuniyoshi KM.Poland-Mobius syndrome and cocaine abuse: a relook at vascular etiology. Pediatr Neurol 2005;32:285-287. PMID: 15797189 58. Puvabanditsin S, Garrow E, Rabi FA, Titapiwatanakun R, Kuniyoshi KM. Partial trisomy 8q and partial monosomy 18p: a case report. Ann Genet. 2004;4:285-287. PMID: 15581839 59. Puvabanditsin S, Garrow E, Sitburana O, Avila FM, Nabong MY, Biswas A. Syngnathia and Van der Woude syndrome: A case report and literature review. Cleft Palate Craniofac J. 2003;40:104-106. PMID: 12498614 60. Puvabanditsin S, Garrow E, Anjali B, Davydov A, Gomez M, Liangthanasarn P. Congenital partial pericardial defect in a neonate: a case report. Am J Perinatol 2003;20:121-123. PMID: 12802711 61. Puvabanditsin S, Garrow E, Applewhite L, Akpalu D, Quizon MC. Intracranial lipomas in neonate. J Perinatol. 2002;22:414-415. PMID: 12082480 62. Puvabanditsin S, Garrow E, Zia-Ullah M, Supavekin S, Lianthanasarn P, Denev KI. Monosomy 11Q: report of new phenotypic manifestations. Genet Couns. 2001;12:283-286. PMID: 11693793 63. Puvabanditsin S, Garrow E, Dae Un Kim, Tirakitsoontorn P, Luan J. Junctional epidermolysis bullosa associated with congenital localized absence of skin, and pyloric atresia in two newborn siblings. J Am Acad Dermatol. 2001;44(2 Suppl):330-335. PMID: 11174408 64. Puvabanditsin S, Garrow E, Biswas A, Punyasavasut N. Congenital lobar emphysema. J Cardiovasc Surg (Torino) 2000;41:953-956. PMID: 11232983 65. Puvabanditsin S, Garrow E, Samransamraujkit R, Lopez LA, Lambert WC. Epidermolysis bullosa associated with CLAS, fetal abdominal mass, and pyloric atresia. Pediatr Dermatol. 1997;14:359-362. PMID: 9336805 66. Puvabanditsin S, Wojdylo EW, Garrow E, Kalavantavanich K. Group B streptococcal meningitis: a case of transverse myelitis with spinal cord and posterior fossa cysts. Pediatr Radiol. 1997;27:317-318. PMID: 9094237 67. Puvabanditsin S, Garrow E, Samransamraujkit R,Lopez LA. Postnatal intussusception in premature infant causing jejunal atresia. J Pediatr Surg. 1996;31:711-712. PMID: 8861489 68. Puvabanditsin S, Garrow E, Vizarra R. An unusual cause of congenital ascites. Acta Paediatr 1995;84:829-830 PMID: 7549310