Congenital defects / diseases
09 Oct 2014 : Case report 
Annular Pancreas: A Cause of Gastric Outlet Obstruction in a 20-Year-Old Patient
Raha Alahmadi, Saud Almuhammadi
DOI: 10.12659/AJCR.891041
Am J Case Rep 2014; 15:437-440
1,214 24 7
09 Oct 2014 : Case report
Annular Pancreas: A Cause of Gastric Outlet Obstruction in a 20-Year-Old Patient
Raha Alahmadi, Saud Almuhammadi
DOI: 10.12659/AJCR.891041
Am J Case Rep 2014; 15:437-440
1214 24 7
20 Sep 2014 : Case report 
Horizontal Liver Cleft: A Rare Anatomic Variant
Yong Han Ting, Kian Soon Lim
DOI: 10.12659/AJCR.892274
Am J Case Rep 2014; 15:401-403
1,288 13 1
20 Sep 2014 : Case report
Horizontal Liver Cleft: A Rare Anatomic Variant
Yong Han Ting, Kian Soon Lim
DOI: 10.12659/AJCR.892274
Am J Case Rep 2014; 15:401-403
1288 13 1
04 Aug 2014 : Case report 
Medical Treatment of an Adult with Uncorrected Isolated Interrupted Aorta Resulted in no Complications after 4 Years of Follow-Up
Ali Öztürk, Emin Evren Özcan, Erdem Özel, Samet Uyar, Ömer Şenaslan
DOI: 10.12659/AJCR.890716
Am J Case Rep 2014; 15:330-332
889 11 2
04 Aug 2014 : Case report
Medical Treatment of an Adult with Uncorrected Isolated Interrupted Aorta Resulted in no Complications after 4 Years of Follow-Up
Ali Öztürk, Emin Evren Özcan, Erdem Özel, Samet Uyar, Ömer Şenaslan
DOI: 10.12659/AJCR.890716
Am J Case Rep 2014; 15:330-332
889 11 2
05 Jul 2014 : Case report
Recurrent Epistaxis Caused by an Intranasal Supernumerary Tooth in a Young Adult
Hamed O. Al Dhafeeri, Abdulmajid Kavarodi, Khalil Al Shaikh, Ahmed Bukhari, Omair Al Hussain, Ahmed El Baramawy
DOI: 10.12659/AJCR.890710
Am J Case Rep 2014; 15:291-293
2,102 24 8
05 Jul 2014 : Case report
Recurrent Epistaxis Caused by an Intranasal Supernumerary Tooth in a Young Adult
Hamed O. Al Dhafeeri, Abdulmajid Kavarodi, Khalil Al Shaikh, Ahmed Bukhari, Omair Al Hussain, Ahmed El Baramawy
DOI: 10.12659/AJCR.890710
Am J Case Rep 2014; 15:291-293
2102 24 8
26 Jun 2014 : Case report 
The role of the new Valeo stent for treating pulmonary artery stenoses in children with complex cardiac malformations
Nikhil Sharma, Sebastian Goreczny
DOI: 10.12659/AJCR.890455
Am J Case Rep 2014; 15:275-279
1,284 11 2
26 Jun 2014 : Case report
The role of the new Valeo stent for treating pulmonary artery stenoses in children with complex cardiac malformations
Nikhil Sharma, Sebastian Goreczny
DOI: 10.12659/AJCR.890455
Am J Case Rep 2014; 15:275-279
1284 11 2
10 Jun 2014 : Case report 
Slit ventricle syndrome and early-onset secondary craniosynostosis in an infant
Hyun Gee Ryoo, Seung-Ki Kim, Jung-Eun Cheon, Ji Yeoun Lee, Kyu-Chang Wang, Ji Hoon Phi
DOI: 10.12659/AJCR.890590
Am J Case Rep 2014; 15:246-253
1,621 21 3
10 Jun 2014 : Case report
Slit ventricle syndrome and early-onset secondary craniosynostosis in an infant
Hyun Gee Ryoo, Seung-Ki Kim, Jung-Eun Cheon, Ji Yeoun Lee, Kyu-Chang Wang, Ji Hoon Phi
DOI: 10.12659/AJCR.890590
Am J Case Rep 2014; 15:246-253
1621 21 3
07 May 2014 : Case report 
Pallister-Killian syndrome
Aarthi Srinivasan, Debra Wright
DOI: 10.12659/AJCR.890614
Am J Case Rep 2014; 15:194-198
1,638 32 4
07 May 2014 : Case report
Pallister-Killian syndrome
Aarthi Srinivasan, Debra Wright
DOI: 10.12659/AJCR.890614
Am J Case Rep 2014; 15:194-198
1638 32 4
02 May 2014 : Case report
Gallbladder agenesis with a primary choledochal stone in a patient with situs inversus totalis
Hassan A. Alzahrani, Nizar M. Yamani
DOI: 10.12659/AJCR.890523
Am J Case Rep 2014; 15:185-188
1,136 10 4
02 May 2014 : Case report
Gallbladder agenesis with a primary choledochal stone in a patient with situs inversus totalis
Hassan A. Alzahrani, Nizar M. Yamani
DOI: 10.12659/AJCR.890523
Am J Case Rep 2014; 15:185-188
1136 10 4
28 Mar 2014 : Case report 
Autologous bone marrow mononuclear cell transplantation in Duchenne muscular dystrophy
Alok Sharma, Hemangi Sane, Amruta Paranjape, Khushboo Bhagwanani, Nandini Gokulchandran, Prerna Badhe
DOI: 10.12659/AJCR.890078
Am J Case Rep 2014; 15:128-134
1,672 20 12
28 Mar 2014 : Case report
Autologous bone marrow mononuclear cell transplantation in Duchenne muscular dystrophy
Alok Sharma, Hemangi Sane, Amruta Paranjape, Khushboo Bhagwanani, Nandini Gokulchandran, Prerna Badhe
DOI: 10.12659/AJCR.890078
Am J Case Rep 2014; 15:128-134
1672 20 12
18 Mar 2014 : Case report 
Congenital arhinia: A rare case
Mao-mao Zhang, Yang-hong Hu, Wei He, Kui-kui Hu
DOI: 10.12659/AJCR.890072
Am J Case Rep 2014; 15:115-118
2,678 30 2
18 Mar 2014 : Case report
Congenital arhinia: A rare case
Mao-mao Zhang, Yang-hong Hu, Wei He, Kui-kui Hu
DOI: 10.12659/AJCR.890072
Am J Case Rep 2014; 15:115-118
2678 30 2
07 Mar 2014 : Case report
Multifocal tumoral calcinosis in a 4-year-old girl
Ilyas Sayar, Kemal Peker, Alparslan Kapısız, Isıl Esen Bostancı, Mehmet Gürbüzel, Arda Isik, Necla Aydın Peker
DOI: 10.12659/AJCR.890166
Am J Case Rep 2014; 15:103-106
947 12 0
07 Mar 2014 : Case report
Multifocal tumoral calcinosis in a 4-year-old girl
Ilyas Sayar, Kemal Peker, Alparslan Kapısız, Isıl Esen Bostancı, Mehmet Gürbüzel, Arda Isik, Necla Aydın Peker
DOI: 10.12659/AJCR.890166
Am J Case Rep 2014; 15:103-106
947 12 0
23 Jan 2014 : Case report
Phenotype-genotype discordance in congenital malformations with communication disorders resembling trisomy 18 (Edwards syndrome)
Antoni Pruszewicz, Bożena Wiskirska - Woźnica, Waldemar Wojnowski, Hanna Czerniejewska, Joanna Jackowska, Małgorzata Jarmuż, Krzysztof Szyfter, Małgorzata Leszczyńska
DOI: 10.12659/AJCR.884033
Am J Case Rep 2014; 15:41-44
1,785 19 2
23 Jan 2014 : Case report
Phenotype-genotype discordance in congenital malformations with communication disorders resembling trisomy 18 (Edwards syndrome)
Antoni Pruszewicz, Bożena Wiskirska - Woźnica, Waldemar Wojnowski, Hanna Czerniejewska, Joanna Jackowska, Małgorzata Jarmuż, Krzysztof Szyfter, Małgorzata Leszczyńska
DOI: 10.12659/AJCR.884033
Am J Case Rep 2014; 15:41-44
1785 19 2
17 Jan 2014 : Case report
Total hip replacement for an ochronotic patient: A technical trick
Oguz Cebesoy, Mustafa Isik, Mehmet Subasi, Abbas Kaya, Fethi Bilgin, Oğuz Kaya
DOI: 10.12659/AJCR.890008
Am J Case Rep 2014; 15:27-30
918 16 1
17 Jan 2014 : Case report
Total hip replacement for an ochronotic patient: A technical trick
Oguz Cebesoy, Mustafa Isik, Mehmet Subasi, Abbas Kaya, Fethi Bilgin, Oğuz Kaya
DOI: 10.12659/AJCR.890008
Am J Case Rep 2014; 15:27-30
918 16 1
13 Dec 2013 : Case report
Biventricular non-compaction with predominant right ventricular involvement, reduced left ventricular systolic and diastolic function, and pulmonary hypertension in a Hispanic male
Sarmad Said, Chad J. Cooper, Karla Quevedo, Emmanuel Rodriguez, German T. Hernandez
DOI: 10.12659/AJCR.889676
Am J Case Rep 2013; 14:539-542
1,379 15 6
13 Dec 2013 : Case report
Biventricular non-compaction with predominant right ventricular involvement, reduced left ventricular systolic and diastolic function, and pulmonary hypertension in a Hispanic male
Sarmad Said, Chad J. Cooper, Karla Quevedo, Emmanuel Rodriguez, German T. Hernandez
DOI: 10.12659/AJCR.889676
Am J Case Rep 2013; 14:539-542
1379 15 6
02 Oct 2013 : Case report
Double superior vena cava on fistulogram: A case report and discussion
Chad J. Cooper, Anwar Soliman Gerges, Emmanuel Anekwe, German T. Hernandez
DOI: 10.12659/AJCR.889589
Am J Case Rep 2013; 14:395-397
822 10 3
02 Oct 2013 : Case report
Double superior vena cava on fistulogram: A case report and discussion
Chad J. Cooper, Anwar Soliman Gerges, Emmanuel Anekwe, German T. Hernandez
DOI: 10.12659/AJCR.889589
Am J Case Rep 2013; 14:395-397
822 10 3
16 Sep 2013 : Case report 
Bland-White-Garland syndrome – a rare and serious cause of failure to thrive
Agnieszka Szmigielska, Maria Roszkowska-Blaim, Małgorzata Gołąbek-Dylewska, Agnieszka Tomik, Michał Brzewski, Bożena Werner
DOI: 10.12659/AJCR.889112
Am J Case Rep 2013; 14:370-372
1,706 12 4
16 Sep 2013 : Case report
Bland-White-Garland syndrome – a rare and serious cause of failure to thrive
Agnieszka Szmigielska, Maria Roszkowska-Blaim, Małgorzata Gołąbek-Dylewska, Agnieszka Tomik, Michał Brzewski, Bożena Werner
DOI: 10.12659/AJCR.889112
Am J Case Rep 2013; 14:370-372
1706 12 4
05 Sep 2012 : Case report
Infantile hypotonia with failure to thrive
Mohamed Nagiub, Karen Alton, Premchand Anne
DOI: 10.12659/AJCR.883367
Am J Case Rep 2012; 13:214-217
790 8 0
05 Sep 2012 : Case report
Infantile hypotonia with failure to thrive
Mohamed Nagiub, Karen Alton, Premchand Anne
DOI: 10.12659/AJCR.883367
Am J Case Rep 2012; 13:214-217
790 8 0
09 Jul 2012 : Case report
Major liver resection by a hanging maneuver for an infant with hepatoblastoma
Megumi Kobayashi, Masaru Mizuno, Yasushi Hasegawa, Hiroyuki Nitta, Go Wakabayashi
DOI: 10.12659/AJCR.883241
Am J Case Rep 2012; 13:140-142
884 7 1
09 Jul 2012 : Case report
Major liver resection by a hanging maneuver for an infant with hepatoblastoma
Megumi Kobayashi, Masaru Mizuno, Yasushi Hasegawa, Hiroyuki Nitta, Go Wakabayashi
DOI: 10.12659/AJCR.883241
Am J Case Rep 2012; 13:140-142
884 7 1
14 Sep 2012 : Case report
Type IV neonatal Bartter syndrome complicated with congenital chloride diarrhea
Hale Sakallı, Hakan Bucak
DOI: 10.12659/AJCR.883446
Am J Case Rep 2012; 13:230-233
1,408 14 0
14 Sep 2012 : Case report
Type IV neonatal Bartter syndrome complicated with congenital chloride diarrhea
Hale Sakallı, Hakan Bucak
DOI: 10.12659/AJCR.883446
Am J Case Rep 2012; 13:230-233
1408 14 0
13 Jun 2012 : Case report
Diagnosis of chromosomal abnormalities in a patient with thanatophoric dysplasia (TD) type I: The first report describing an important association between cytogenetic findings and TD
Mehmet Turgut, Osman Demirhan, Erdal Tunç, Ibrahim Hakan Bucak, Perihan Yasemen Canoz, Fatih Temiz, Gokhan Tumgor
DOI: 10.12659/AJCR.883026
Am J Case Rep 2012; 13:109-113
1,025 13 1
13 Jun 2012 : Case report
Diagnosis of chromosomal abnormalities in a patient with thanatophoric dysplasia (TD) type I: The first report describing an important association between cytogenetic findings and TD
Mehmet Turgut, Osman Demirhan, Erdal Tunç, Ibrahim Hakan Bucak, Perihan Yasemen Canoz, Fatih Temiz, Gokhan Tumgor
DOI: 10.12659/AJCR.883026
Am J Case Rep 2012; 13:109-113
1025 13 1
10 Jul 2012 : Case report
Permanent neonatal diabetes mellitus
Abdulrahman Al-Matary, Mushtaq Hussain, Ahmed Nahari, Jaffar Ali
DOI: 10.12659/AJCR.883242
Am J Case Rep 2012; 13:143-145
1,232 13 3
10 Jul 2012 : Case report
Permanent neonatal diabetes mellitus
Abdulrahman Al-Matary, Mushtaq Hussain, Ahmed Nahari, Jaffar Ali
DOI: 10.12659/AJCR.883242
Am J Case Rep 2012; 13:143-145
1232 13 3
13 Jun 2012 : Case report
The first case of Horn Kolb Syndrome in Turkey, diagnosed prenatally at the 23rd week of a pregnancy: A very rare and unusual case far from the original geography
Ismail Temur, Kahraman Ulker, Islim Volkan, Mehmet Karaca, Mustafa Ersoz, Abdulaziz Gul, Esat Adiguzel
DOI: 10.12659/AJCR.883025
Am J Case Rep 2012; 13:106-108
2,522 11 3
13 Jun 2012 : Case report
The first case of Horn Kolb Syndrome in Turkey, diagnosed prenatally at the 23rd week of a pregnancy: A very rare and unusual case far from the original geography
Ismail Temur, Kahraman Ulker, Islim Volkan, Mehmet Karaca, Mustafa Ersoz, Abdulaziz Gul, Esat Adiguzel
DOI: 10.12659/AJCR.883025
Am J Case Rep 2012; 13:106-108
2522 11 3
29 Dec 2011 : Case report
Scleritis in association with Wiskott-Aldrich syndrome
Vasileios Karampatakis, Kordali Panagiota, Diamantis Almaliotis, Maria Hatzistilianou
DOI: 10.12659/AJCR.882211
Am J Case Rep 2011; 12:210-212
825 13 1
29 Dec 2011 : Case report
Scleritis in association with Wiskott-Aldrich syndrome
Vasileios Karampatakis, Kordali Panagiota, Diamantis Almaliotis, Maria Hatzistilianou
DOI: 10.12659/AJCR.882211
Am J Case Rep 2011; 12:210-212
825 13 1
06 Dec 2011 : Case report
SED-brachydactyly and distinctive speech: Report of a new familial cas
Camila Ive Ferreira Oliveira, Guaracy Carvalho Filho, Antonio Soares Souza, Agnes Cristina Fett-Conte
DOI: 10.12659/AJCR.882136
Am J Case Rep 2011; 12:189-194
1,692 10 0
06 Dec 2011 : Case report
SED-brachydactyly and distinctive speech: Report of a new familial cas
Camila Ive Ferreira Oliveira, Guaracy Carvalho Filho, Antonio Soares Souza, Agnes Cristina Fett-Conte
DOI: 10.12659/AJCR.882136
Am J Case Rep 2011; 12:189-194
1692 10 0
18 Oct 2011 : Case report
Brugada syndrome revealed by propafenone administration
Murat Turfan, Ethem Celik, Ender Ornek, Sani Namık Murat, Mustafa Duran, Muhammed Bora DemirCelik
DOI: 10.12659/AJCR.882016
Am J Case Rep 2011; 12:122-124
1,042 20 0
18 Oct 2011 : Case report
Brugada syndrome revealed by propafenone administration
Murat Turfan, Ethem Celik, Ender Ornek, Sani Namık Murat, Mustafa Duran, Muhammed Bora DemirCelik
DOI: 10.12659/AJCR.882016
Am J Case Rep 2011; 12:122-124
1042 20 0
In Press
22 Mar 2024 : Case report 
Am J Case Rep In Press; DOI: 10.12659/AJCR.943346
24 Mar 2024 : Case report 
Am J Case Rep In Press; DOI: 10.12659/AJCR.943560
26 Mar 2024 : Case report 
Am J Case Rep In Press; DOI: 10.12659/AJCR.943893
27 Mar 2024 : Case report 
Am J Case Rep In Press; DOI: 10.12659/AJCR.942126
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