Congenital lobar emphysema presenting at late childhood: A rare case report
Abstract
1. Omaha, Nebr., USA Cremers Cor WRJ, Smith RJH (eds). Genetic Hearing Impairment. Adv Otorhinolaryngol. Basel, Karger, 2002, vol 61, pp 184‐91. 2. Usher C. On the inheritance of retinitis pigmentosa with note of cases. Roy London Ophthalniol Hosp Rep 1914;14:130‐6. 3. Mets MB, Young NM, Pass A, Lasky JB. Early diagnosis of Usher syndrome in children. Trans Am Ophthalmo Soc 2000;98:237‐45. 4. Bonneau D, Raymond F, Kremer C, Klossek JM, Kaplan J, Patte F. Usher syndrome type I associated with bronchiectasis and immotile nasal cilia in two brothers. J Med Genet 1993;30:253‐4. 5. Armengot M1, Salom D, Diaz‐Llopis M, Millan JM, Milara J, Mata M, et al. Nasal Ciliary Beat Frequency and Beat Pattern in Retinal Ciliopathies. Invest Ophthalmol Vis Sci 2012;53:2076‐9.
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