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Poland's Syndrome

Radiology, 1971
The combined congenital malformation of partial or complete absence of the pectoralis major muscle and webbing of the fingers, on the same side, was first described by Poland in 1841. Ten percent of patients with syndactylism have the combined anomaly. The breast and nipple may be hypoplastic or absent.
F S, Brooksaler, L, Graivier
exaly   +5 more sources

Poland's Syndrome

Chest Surgery Clinics of North America, 2000
Poland's syndrome is characterized by hypoplasia or absence of the breast or nipple, hypoplasia of subcutaneous tissue, absence of the costosternal portion of the pectoralis major muscle, absence of the pectoralis minor muscle, and absence of costal cartilages or ribs 2, 3, and 4 or 3, 4, and 5.
R, Slezak, M, Sasiadek
openaire   +4 more sources

Poland’s Syndrome

2020
Poland’s syndrome is a sporadic, congenital thoracic deformity, mostly unilateral with a wide spectrum of presentation. According to the vascular theory, most likely the syndrome is caused by a defect of blood supply in the subclavian system that causes hypoplasia of the subclavian artery or one of its branches during the sixth to seventh weeks of ...
Di Lorenzo, S.   +2 more
openaire   +1 more source

Poland-Syndrom

Klinische Pädiatrie, 1983
We present two patients with symptoms typical of Poland's Syndrome: unilateral hypoplasia of the pectoral muscle and dysplastic anomalies of the ipsilateral upper limb. Additionally skeletal and G.U. tract abnormalities can be found. One of our cases shows stenosis of the ureterovesical junction which led to hydronephrosis and dilation of the ureter ...
A, Oppolzer, M, Sacher
openaire   +2 more sources

Poland’s syndrome revisited

The Annals of Thoracic Surgery, 2002
Poland's syndrome is a rare congenital anomaly characterized by unilateral chest wall hypoplasia and ipsilateral hand abnormalities. Literary data suggest its sporadic nature. The prevailing theory of its cause is hypoplasia of the subclavian artery or its branches, which may lead to a range of developmental changes.
Alexander A, Fokin, Francis, Robicsek
openaire   +2 more sources

Poland Syndrome

Seminars in Thoracic and Cardiovascular Surgery, 2009
Poland syndrome is characterized by hypoplasia or absence of the breast or nipple, hypoplasia of subcutaneous tissue, absence of the costosternal portion of the pectoralis major muscle, absence of the pectoralis minor muscle, and absence of costal cartilages or ribs 2, 3, and 4 or 3, 4, and 5.
openaire   +2 more sources

Poland’s Syndrome

2009
Ever since Poland described a group of anomalies with absence of the pectoralis major and minor muscles and syndactyly of the ipsilateral hand, many variations of this condition have been reported in the literature. Thomson, in 1895, added other features, including the absence of ribs, chest wall depression, amastia with or without athelia, the absence
Renato Da Silva Freitas   +4 more
openaire   +1 more source

Poland’s Syndrome

2016
Poland’s Syndrome, in the classic sense, is the unilateral absence of the sternocostal head of the pectoralis major muscle, ipsilateral breast hypoplasia, and a concomitant, ipsilateral hand deformity. The syndrome has since evolved to encompass a myriad of anomalies, which rarely present collectively in the same individual.
Alessandro G. Cusano, Michael S. Wong
openaire   +1 more source

Poland’s Syndrome

2017
The Poland´s Syndrome (PS) was initially described for Alfred Poland in 1941 and is characterized for a set of congenital alterations that involves the chest wall and the ipsilateral superior member in different severity cases. It is a rare illness whose etiology still is unknown.
Ricardo Cavalcanti Ribeiro   +2 more
openaire   +1 more source

Poland's syndrome [Poland sendromu]

2011
Poland's syndrome (PS) is a rarely encountered congenital disorder that is characterised with absence of pectoralis major muscle. However, hand and other organ anomalies may accompany the syndrome. It is usually right sided. We report the left sided two PS cases.
Koplay M., Bulut I., Kantarci M.
openaire   +1 more source

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