Kartagener's syndrome (KS) is an autosomal recessive subgroup of primary ciliary dyskinesia (PCD) which presents as sinusitis, bronchiectasis, and dextrocardia .The deficit in the coordination of ciliary motion results in mucus retention and recurrent respiratory tract infections (sinusitis, otitis media and pneumonia. Kartagener patients are more or less troubled by repeated infection for which they have to seek medical attention which is largely the reason for their morbidity .An adult person commonly seeks medical help because of infertility .We present series of three cases of Kartagener syndrome with characteristic clinico-radiological features
BACKGROUND: Recurrent lower respiratory tract infection (LRTI) is a very common problem we encounter...
Kartagener syndrome is a rare genetic disorder which includes a triad of bronchiectasis, chronic sin...
AbstractKartagener’s syndrome is a rare congenital disorder consisting of sinusitis, bronchiectasis ...
Kartagener Syndrome is a rare autosomal recessive disorder consisting of triad of sinusitis, bronchi...
Introduction: This article addresses the general aspects (pathophysiology, embryology, clinical pres...
Primary ciliary dyskinesia (PCD), previously known as immotile cilia syndrome, is an autosomal reces...
Kartagener’s syndrome is a rare congenital disorder consisting of situs inversus, bronchiectasis and...
Summary: Kartagener syndrome (KS), also known as immotile cilia syndrome or as a primary ciliary dys...
Abstract Background Kartagener’s syndrome is a subset of primary ciliary dyskinesia, an autosomal re...
artagener’s syndrome is an autosomal recessive disorder. It is a subset of primary ciliary dyskinesi...
Kartagener syndrome is an autosomic recessive hereditary disease characterized of primary ciliary dy...
Kartagener’s syndrome is defined as motility dysfunction of the epithelial cilia lining the respirat...
Kartagener's syndrome has been noticed since Max Kartagener had reported eleven cases with chronic s...
APSRワークショップ (APSR Workshop)The clinical features, ciliary function and ultrastructure in Kartagener'...
Primary ciliary dyskinesias (PCD) are rare genetic diseases with autosomal recessive transmission, a...
BACKGROUND: Recurrent lower respiratory tract infection (LRTI) is a very common problem we encounter...
Kartagener syndrome is a rare genetic disorder which includes a triad of bronchiectasis, chronic sin...
AbstractKartagener’s syndrome is a rare congenital disorder consisting of sinusitis, bronchiectasis ...
Kartagener Syndrome is a rare autosomal recessive disorder consisting of triad of sinusitis, bronchi...
Introduction: This article addresses the general aspects (pathophysiology, embryology, clinical pres...
Primary ciliary dyskinesia (PCD), previously known as immotile cilia syndrome, is an autosomal reces...
Kartagener’s syndrome is a rare congenital disorder consisting of situs inversus, bronchiectasis and...
Summary: Kartagener syndrome (KS), also known as immotile cilia syndrome or as a primary ciliary dys...
Abstract Background Kartagener’s syndrome is a subset of primary ciliary dyskinesia, an autosomal re...
artagener’s syndrome is an autosomal recessive disorder. It is a subset of primary ciliary dyskinesi...
Kartagener syndrome is an autosomic recessive hereditary disease characterized of primary ciliary dy...
Kartagener’s syndrome is defined as motility dysfunction of the epithelial cilia lining the respirat...
Kartagener's syndrome has been noticed since Max Kartagener had reported eleven cases with chronic s...
APSRワークショップ (APSR Workshop)The clinical features, ciliary function and ultrastructure in Kartagener'...
Primary ciliary dyskinesias (PCD) are rare genetic diseases with autosomal recessive transmission, a...
BACKGROUND: Recurrent lower respiratory tract infection (LRTI) is a very common problem we encounter...
Kartagener syndrome is a rare genetic disorder which includes a triad of bronchiectasis, chronic sin...
AbstractKartagener’s syndrome is a rare congenital disorder consisting of sinusitis, bronchiectasis ...