Add to ORKGA 13-year-old female has been suffering from chronic sinusitis and bilateral otitis media with effusion since her early childhood. She has been pointed out situs inversus. Transmission electron microscopic examination of nasal mucosa confirmed a lack of inner dynein arm of nasal cilia, and she was diagnosed as having Kartagener's syndrome. She underwent endoscopic sinus surgery for chronic sinusitis and myringoplasty for a perforation of the right tympanic membrane caused by tympanostomy tube insertion. Chronic sinusitis accompanied by Kartagener's syndrome is discussed in relation to surgical management
Kartagener's syndrome, also called primary ciliary dyskinesia, is an autosomal recessive genetic ent...
AbstractKartagener’s syndrome is a rare congenital disorder consisting of sinusitis, bronchiectasis ...
BACKGROUND: Recurrent lower respiratory tract infection (LRTI) is a very common problem we encounter...
A case of Kartagener's syndrome in a 21-year-old female was reported. Her complaints were persistent...
Kartagener's syndrome has been noticed since Max Kartagener had reported eleven cases with chronic s...
Background: Kartagener syndrome (KS) is a rare congenital disease characterised by a clinical triad ...
The nasal polyposis is a chronic inflammatory process of the nasal mucosa. Although it is rare in ch...
Introduction: This article addresses the general aspects (pathophysiology, embryology, clinical pres...
Kartagener's syndrome (KS) is an autosomal recessive subgroup of primary ciliary dyskinesia (PCD) wh...
AbstractA White, 48-year-old woman, natural from Uberaba-MG, presented herself to hospital. She had ...
Abstract Background Kartagener’s syndrome is a subset of primary ciliary dyskinesia, an autosomal re...
Nedaa Skeik1–3, Fadi I Jabr41Mayo Clinic, Rochester, MN, USA; 2Dartmouth Medical School, H...
Kartagener Syndrome is a rare autosomal recessive disorder consisting of triad of sinusitis, bronchi...
Kartagener’s Syndrome is a rare congenital malformation andcharacterized by the triad of bronchiecta...
The triad of situs inversus totalis, bronchiectasis and sinusitis is known as Kartagener syndrome wh...
Kartagener's syndrome, also called primary ciliary dyskinesia, is an autosomal recessive genetic ent...
AbstractKartagener’s syndrome is a rare congenital disorder consisting of sinusitis, bronchiectasis ...
BACKGROUND: Recurrent lower respiratory tract infection (LRTI) is a very common problem we encounter...
A case of Kartagener's syndrome in a 21-year-old female was reported. Her complaints were persistent...
Kartagener's syndrome has been noticed since Max Kartagener had reported eleven cases with chronic s...
Background: Kartagener syndrome (KS) is a rare congenital disease characterised by a clinical triad ...
The nasal polyposis is a chronic inflammatory process of the nasal mucosa. Although it is rare in ch...
Introduction: This article addresses the general aspects (pathophysiology, embryology, clinical pres...
Kartagener's syndrome (KS) is an autosomal recessive subgroup of primary ciliary dyskinesia (PCD) wh...
AbstractA White, 48-year-old woman, natural from Uberaba-MG, presented herself to hospital. She had ...
Abstract Background Kartagener’s syndrome is a subset of primary ciliary dyskinesia, an autosomal re...
Nedaa Skeik1–3, Fadi I Jabr41Mayo Clinic, Rochester, MN, USA; 2Dartmouth Medical School, H...
Kartagener Syndrome is a rare autosomal recessive disorder consisting of triad of sinusitis, bronchi...
Kartagener’s Syndrome is a rare congenital malformation andcharacterized by the triad of bronchiecta...
The triad of situs inversus totalis, bronchiectasis and sinusitis is known as Kartagener syndrome wh...
Kartagener's syndrome, also called primary ciliary dyskinesia, is an autosomal recessive genetic ent...
AbstractKartagener’s syndrome is a rare congenital disorder consisting of sinusitis, bronchiectasis ...
BACKGROUND: Recurrent lower respiratory tract infection (LRTI) is a very common problem we encounter...