An atypical type of alveolar capillary dysplasia in a 3‐month‐old infant

2021 ◽  
Vol 63 (3) ◽  
pp. 350-352
Author(s):  
Kenji Miyamoto ◽  
Yoshimasa Nakazato ◽  
Masahiro Nakayama ◽  
Shigemi Yoshihara

1997 ◽  
Vol 17 (6) ◽  
pp. 959-975 ◽  
Author(s):  
Sibylle Haraida ◽  
Hannelore Lochbuhler ◽  
A. Heger ◽  
A. Nerlich ◽  
J. Diebold ◽  
...  


2009 ◽  
Vol 5 (2) ◽  
pp. 110-114 ◽  
Author(s):  
Aaron Swenson ◽  
Steven Donn


Author(s):  
Chloé Puisney‐Dakhli ◽  
Francesca Gubana ◽  
François Petit ◽  
Hanane Bouchghoul ◽  
Valérie Gautier ◽  
...  


2001 ◽  
Vol 37 (1) ◽  
pp. 85-86 ◽  
Author(s):  
J. McGaughran ◽  
DJ Souter ◽  
CA Kuschel




2018 ◽  
Vol 46 (1) ◽  
pp. 101-101
Author(s):  
Katharine Robb ◽  
Sook-kyung Kwon ◽  
Veerajalandhar Allareddy ◽  
Aditya Badheka


2018 ◽  
Vol 8 (3) ◽  
pp. 204589401879514 ◽  
Author(s):  
Evelien Slot ◽  
Gabriëla Edel ◽  
Ernest Cutz ◽  
Arno van Heijst ◽  
Martin Post ◽  
...  

Alveolar capillary dysplasia with misalignment of the pulmonary veins (ACD/MPV) is a rare and lethal disorder mainly involving the vascular development of the lungs. Since its first description, significant achievements in research have led to a better understanding of the underlying molecular mechanism of ACD/MPV and genetic studies have identified associations with genomic alterations in the locus of the transcription factor FOXF1. This in turn has increased the awareness among clinicians resulting in over 200 cases reported so far, including genotyping of patients in most recent reports. Collectively, this promoted a better stratification of the patient group, leading to new perspectives in research on the pathogenesis. Here, we provide an overview of the clinical aspects of ACD/MPV, including guidance for clinicians, and review the ongoing research into the complex molecular mechanism causing this severe lung disorder.



2015 ◽  
Vol 52 (11) ◽  
pp. 984-986 ◽  
Author(s):  
Abdul Razak ◽  
Pankaj Kumar Mohanty ◽  
N Karthik Nagesh


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