Talk:Welcome
I was experimenting on using Flow for discussion pages. I don't like it much.
Ehlers-Danlos syndrome type IV (EDS IV) is caused by mutation within the COL3A1 gene, resulting in the disorder of type III procollagen. The diagnosis is confirmed by demonstrating the synthesis of abnormal type III procollagen molecules from cultured dermal fibroblasts or by identifying the mutation in the COL3A1 gene. The authors report a case of EDS IV caused by a novel point mutation in the COL3A1 gene in a 16-yr-old female. Recurrent haemoptysis and cavitary formation of the lung were evidence of pulmonary involvement. However, extrathoracic manifestations of EDS IV were mostly absent. To the best of the authors' knowledge, all previously reported Ehlers-Danlos syndrome IV patients with respiratory disease had the characteristic findings or histories of Ehlers-Danlos syndrome IV. In the present case, connective tissue friability was suspected due to tissue laceration observed in the biopsied lung specimen, and the diagnosis was made beginning from this pivotal finding.
https://erj.ersjournals.com/content/19/1/195
204.187.34.100 (talkcontribsblock)
Superior surface- peritoneal Base: upper part peritoneal Other : non peritoneal Neck is encircled by prostate.
Bladder- Male Urachus Superior surface
Peritoneum Inferolateral surface Urethra
Ejaculatory
Prostate gland
lymphangiectasia of the duodenum, pale yellow to tan flat lesion submucosal appearing, white speckled appearance, not firm at all The lesion is raised and keratinaceous