Vesico‐amniotic shunting for lower urinary tract obstruction in a fetus with VACTERL association
This article is protected by copyright. All rights reserved. (Source: Congenital Anomalies)
Source: Congenital Anomalies - February 29, 2016 Category: Genetics & Stem Cells Authors: Tomonobu Kanasugi, Akihiko Kikuchi, Gen Haba, Yuri Sasaki, Chizuko Isurugi, Rie Oyama, Toru Sugiyama Tags: Case Report Source Type: research
Formation of the circle of Willis during human embryonic development
This article is protected by copyright. All rights reserved. (Source: Congenital Anomalies)
Source: Congenital Anomalies - February 29, 2016 Category: Genetics & Stem Cells Authors: Tetsuya Takakuwa, Teppei Koike, Taiga Muranaka, Chigako Uwabe, Shigehito Yamada Tags: Short Communication Source Type: research
Unilateral occipital condylar dysplasia: 3‐dimensional multidetector CT and MR findings
(Source: Congenital Anomalies)
Source: Congenital Anomalies - February 25, 2016 Category: Genetics & Stem Cells Authors: Do Hyung Lee, Bo‐Kyung Je, Doran Hong, Sang‐Dae Kim, So‐Hee Eun Tags: Note Source Type: research
Regional hypoplasia of somatosensory cortex in growth‐retarded mice (grt/grt)
This article is protected by copyright. All rights reserved. (Source: Congenital Anomalies)
Source: Congenital Anomalies - February 25, 2016 Category: Genetics & Stem Cells Authors: Kazuhiko Sawada, Shigeyoshi Saito, Akari Sugasawa, Chika Sato, Junya Aoyama, Naoko Ohara, Miwa Horiuchi‐Hirose, Tetsuya Kobayashi Tags: Short Communication Source Type: research
Unilateral occipital condylar dysplasia: 3 ‐dimensional multidetector CT and MR findings
(Source: Congenital Anomalies)
Source: Congenital Anomalies - February 24, 2016 Category: Genetics & Stem Cells Authors: Do Hyung Lee, Bo ‐Kyung Je, Doran Hong, Sang‐Dae Kim, So‐Hee Eun Tags: Note Source Type: research
Systemic and maxillofacial characteristics of eleven Japanese children with Russell –Silver syndrome
This article is protected by copyright. All rights reserved. (Source: Congenital Anomalies)
Source: Congenital Anomalies - February 24, 2016 Category: Genetics & Stem Cells Authors: Chiemi Sato, Takuya Ogawa, Risa Tsuge, Momotoshi Shiga, Michiko Tsuji, Yoshiyuki Baba, Kenjiro Kosaki, Keiji Moriyama Tags: Original Article Source Type: research
Congenital omphalocele and cleft palate in two fetuses
(Source: Congenital Anomalies)
Source: Congenital Anomalies - February 11, 2016 Category: Genetics & Stem Cells Authors: Neha Upadhyay, Muralidhar V. Pai, Shalini S. Nayak, Katta M. Girisha, Anju Shukla Tags: Note Source Type: research
Birth outcomes of patients with isolated anorectal malformations: A population‐based case‐control study
Abstract
In most patients affected by isolated anorectal malformation (IARM) the etiology is largely unknown. Thus, the aim of our project was to analyze possible risk factors for IARM. In the first step, birth outcomes of cases with IARM were analyzed on the basis of maternal socio‐demographic variables, and these data are presented in this paper. Gestational age at delivery, birthweight, preterm birth, low birthweight and small for gestational age of cases with IARM were evaluated in the function of maternal age, birth/pregnancy order, marital and employment status of mothers in the population‐based large dataset of ...
Source: Congenital Anomalies - January 11, 2016 Category: Genetics & Stem Cells Authors: Gabor Vermes, Daniel László, Andrew E. Czeizel, Nándor Ács Tags: Original Article Source Type: research
Expression of peptide fragments from proADM and involvement of mitogen‐activated protein kinase signaling pathways in pulmonary remodeling induced by high pulmonary blood flow
In this study, we investigated the roles of the peptide fragments from proadrenomedullin (proADM) such as adrenomedullin (ADM), adrenotensin (ADT), and proadrenomedullin N‐terminal 20 peptide (PAMP) during pulmonary remodeling caused by high pulmonary blood flow, and probed the possible involvement of mitogen‐activated protein kinase (MAPK) signal transduction pathways. Sixteen rat models of PAH were artificially established by surgically connecting the left common carotid artery to the external jugular vein. We subcutaneously injected an extracellular signal‐regulated protein kinase (ERK1/2) inhibitor, PD98059, in e...
Source: Congenital Anomalies - January 11, 2016 Category: Genetics & Stem Cells Authors: Wei Li, Aili Guo, Lijuan Wang, Qingyu Kong, Rong Wang, Li Han, Cuifen Zhao Tags: Original Article Source Type: research
Andrew E. Czeizel, 3 April 1935–10 August 2015
(Source: Congenital Anomalies)
Source: Congenital Anomalies - January 11, 2016 Category: Genetics & Stem Cells Authors: Nándor Ács, Ferenc Bánhidy, Krishnaswami Sankaranarayanan, Zoltan Merhala Tags: Obituary Source Type: research
Issue Information
Development and morphology of the middle ear. The middle ear comprises the ear ossicle(s) and tympanic membrane. Although the jaw and middle ear bones in mammals and diapsids (modern reptiles and birds) are morphologically homologous, the tympanic membrane is attached to non‐homologous elements between them, suggesting that the tympanic membrane evolved independently in the mammalian and diapsid lineages. Further details can be seen in the article by Takechi et al. in this issue. (Source: Congenital Anomalies)
Source: Congenital Anomalies - January 11, 2016 Category: Genetics & Stem Cells Tags: Issue Information Source Type: research
Truncation and microdeletion of EVC/EVC2 with missense mutation of EFCAB7 in Ellis ‐van Creveld syndrome
In conclusion, we detected two novel nonsense mutations and a partial deletion of EVC/EVC2 in two Vietnamese families with EvC. Moreover, we found in one family a missense mutation of EFCAB7, a possible modifier gene in EvC and its related disorders. This article is protected by copyright. All rights reserved. (Source: Congenital Anomalies)
Source: Congenital Anomalies - January 6, 2016 Category: Genetics & Stem Cells Authors: Tran Quynh Nhu Nguyen, Makiko Saitoh, Huu Tung Trinh, Nguyen Minh Thien Doan, Yoko Mizuno, Masafumi Seki, Yusuke Sato, Seishi Ogawa, Masashi Mizuguchi Tags: Original Article Source Type: research
Prevalence of congenital limb defects: data from birth defects registries in 3 provinces in Southern Thailand
In conclusion, the overall prevalence of CLD in the 3 southern Thailand provinces examined was 2.27 per 1,000 births, and syndromic CLD was significantly higher in pregnant women aged ≥35 years than younger pregnant women. This article is protected by copyright. All rights reserved. (Source: Congenital Anomalies)
Source: Congenital Anomalies - January 5, 2016 Category: Genetics & Stem Cells Authors: Somchit Jaruratanasirikul, Boonsin Tangtrakulwanich, Pornruedee Rachatawiriyakul, Hutcha Sriplung, Wannee Limpitikul, Pathikan Dissaneevate, Nattasit Khunnarakpong, Pongsak Tantichantakarun Tags: Original Article Source Type: research
Systemic and maxillofacial characteristics of eleven Japanese children with Russell–Silver syndrome
This article is protected by copyright. All rights reserved. (Source: Congenital Anomalies)
Source: Congenital Anomalies - January 1, 2016 Category: Genetics & Stem Cells Authors: Chiemi Sato, Takuya Ogawa, Risa Tsuge, Momotoshi Shiga, Michiko Tsuji, Yoshiyuki Baba, Kenjiro Kosaki, Keiji Moriyama Tags: Original Article Source Type: research
Integrated care for down syndrome
This article is protected by copyright. All rights reserved. (Source: Congenital Anomalies)
Source: Congenital Anomalies - January 1, 2016 Category: Genetics & Stem Cells Authors: Ni‐Chung Lee, Yin‐Hsiu Chien, Wuh‐Liang Hwu Tags: Mini Review Source Type: research
