Add to ORKGA síndrome de Poland é uma anomalia congênita caracterizada principalmente por hipoplasia ou aplasia da musculatura torácica unilateral e alterações no membro superior ipsilateral. Este caso refere-se a uma paciente do sexo feminino, sem alterações ao exame físico, mostrando a correlação de achados de imagem (mamografia e ressonância magnética) desta condição rara.Poland's syndrome is a congenital pathology characterized by unilateral chest wall hypoplasia or aplasia and ipsilateral hand abnormalities. The authors report a case report of a female patient presenting without changes on physical examination, and show the correlated imaging findings (mammography and magnetic resonance imaging) of this rare condition
ABSTRACT: Forty-three consecutive cases of Poland’s syndrome were analyzed and the relevant lit-erat...
Poland syndrome is a rare congenital syndrome. Most of the reported cases are sporadic, pattern of g...
Poland Anomaly, one of the sporadic congenital disease involves the congenital unilateral absence or...
The Poland's Syndrome (PS) is a rare congenital anomaly diagnosed in 1 out of 100 000 births. PS pr...
Poland’s syndrome was described following the work of Sir Alfred Poland in the 19th century as a che...
Poland syndrome is indeed a rare congenital malformation that can present with various degrees of th...
The syndrome of Poland is a rare congenital malformation, grouping, to varying degrees, musculoskele...
Poland’s syndrome is a rare congenital condition classically characterized by partial or complete ab...
Poland sendromu, göğüs kafesi ve memenin nadir görülen tek taraflı ve doğumsal bir anomalisidir. Ayn...
Poland syndrome comprises a unilateral absence of the large pectoral muscle, ipsilateral symbrachyda...
Poland’s syndrome is a rare congenital anomaly with absence or hypoplasia of major and minor p...
Poland’s syndrome is a sporadic, congenital thoracic deformity, mostly unilateral, with a wide spe...
PURPOSE: Poland syndrome was first described as a deficiency of the pectoral muscle with ipsilateral...
Diverse changes in the morphology and structure of the mammary gland have been described as a result...
Poland syndrome describes the congenital absence of the pectoralis major and minor muscles on one si...
ABSTRACT: Forty-three consecutive cases of Poland’s syndrome were analyzed and the relevant lit-erat...
Poland syndrome is a rare congenital syndrome. Most of the reported cases are sporadic, pattern of g...
Poland Anomaly, one of the sporadic congenital disease involves the congenital unilateral absence or...
The Poland's Syndrome (PS) is a rare congenital anomaly diagnosed in 1 out of 100 000 births. PS pr...
Poland’s syndrome was described following the work of Sir Alfred Poland in the 19th century as a che...
Poland syndrome is indeed a rare congenital malformation that can present with various degrees of th...
The syndrome of Poland is a rare congenital malformation, grouping, to varying degrees, musculoskele...
Poland’s syndrome is a rare congenital condition classically characterized by partial or complete ab...
Poland sendromu, göğüs kafesi ve memenin nadir görülen tek taraflı ve doğumsal bir anomalisidir. Ayn...
Poland syndrome comprises a unilateral absence of the large pectoral muscle, ipsilateral symbrachyda...
Poland’s syndrome is a rare congenital anomaly with absence or hypoplasia of major and minor p...
Poland’s syndrome is a sporadic, congenital thoracic deformity, mostly unilateral, with a wide spe...
PURPOSE: Poland syndrome was first described as a deficiency of the pectoral muscle with ipsilateral...
Diverse changes in the morphology and structure of the mammary gland have been described as a result...
Poland syndrome describes the congenital absence of the pectoralis major and minor muscles on one si...
ABSTRACT: Forty-three consecutive cases of Poland’s syndrome were analyzed and the relevant lit-erat...
Poland syndrome is a rare congenital syndrome. Most of the reported cases are sporadic, pattern of g...
Poland Anomaly, one of the sporadic congenital disease involves the congenital unilateral absence or...