Generic placeholder image

Current Respiratory Medicine Reviews

Editor-in-Chief

ISSN (Print): 1573-398X
ISSN (Online): 1875-6387

Review Article

Genetic Anomalies of the Respiratory Tract

Author(s): Caterina Cuppari*, Maria Concetta Cutrupi, Annamaria Salpietro, Alessia Sallemi, Monica Fusco, Giuseppe Fabio Parisi and Carmelo Salpietro

Volume 15, Issue 3, 2019

Page: [221 - 230] Pages: 10

DOI: 10.2174/1573398X15666191022100525

conference banner
Abstract

Hereditary lung diseases can affect the airways, parenchyma and vasculature of the lung. Such diseases comprehend simple monogenic disorders such as Kartagener syndrome and α1-antitrypsin deficiency, in which mutations of critical genes are sufficient to induce well‐defined disease phenotypes. A major comprehension of the genetic basis of pulmonary diseases has produced new investigations into their underlying pathophysiology and contributed sometimes to clarify on more frequent sporadic forms. The presence of these structural abnormalities of the respiratory tract can be fatal, so that the identification of causative genes has allowed prenatal diagnosis for many diseases giving a greater hope of survival thanks to a more adequate and prompt management.

Keywords: Airways diseases, alpha-1 antitrypsin deficiency, asthma, cystic fibrosis, dyskinesia, hereditary lung diseases, kartagener syndrome, respiratory tract.

Graphical Abstract
[1]
Sivan Y, Ben-Ari J, Soferman R, DeRowe A. Diagnosis of laryngomalacia by fiberoptic endoscopy: awake compared with anesthesia-aided technique. Chest 2006; 130(5): 1412-8.
[http://dx.doi.org/10.1378/chest.130.5.1412] [PMID: 17099018]
[2]
Richter GT, Thompson DM. The surgical management of laryngomalacia. Otolaryngol Clin North Am 2008; 41(5): 837-64. p.vii.
[http://dx.doi.org/10.1016/j.otc.2008.04.011] [PMID: 18775337]
[3]
Chen JL, Messner AH, Chang KW. Familial laryngomalacia in two siblings with syndromic features. Int J Pediatr Otorhinolaryngol 2006; 70(9): 1651-5.
[http://dx.doi.org/10.1016/j.ijporl.2006.04.010] [PMID: 16774790]
[4]
Shatla ES, Prashanth GP, Aguiar R, Shivalingam G, Al Haq AA. Neonatal stridor in familial congenital laryngeal paralysis (Plott syndrome): A case study in an Omani family. Oman Med J 2017; 32(6): 515-7.
[http://dx.doi.org/10.5001/omj.2017.98] [PMID: 29218130]
[5]
de Groot-van der Mooren MD, Haak MC, Lakeman P, et al. Tracheal agenesis: approach towards this severe diagnosis. Case report and review of the literature. Eur J Pediatr 2012; 171(3): 425-31.
[http://dx.doi.org/10.1007/s00431-011-1563-x] [PMID: 21918809]
[6]
Boogaard R, Huijsmans SH, Pijnenburg MWH, Tiddens HA, de Jongste JC, Merkus PJ. Tracheomalacia and bronchomalacia in children: incidence and patient characteristics. Chest 2005; 128(5): 3391-7.
[http://dx.doi.org/10.1378/chest.128.5.3391] [PMID: 16304290]
[7]
Masters IB, Chang AB, Patterson L, et al. Series of laryngomalacia, tracheomalacia, and bronchomalacia disorders and their associations with other conditions in children. Pediatr Pulmonol 2002; 34(3): 189-95.
[http://dx.doi.org/10.1002/ppul.10156] [PMID: 12203847]
[8]
Wittenborg MH, Gyepes MT, Crocker D. Tracheal dynamics in infants with respiratory distress, stridor, and collapsing trachea. Radiology 1967; 88(4): 653-62.
[http://dx.doi.org/10.1148/88.4.653] [PMID: 6020927]
[9]
Pan W, Peng D, Luo J, et al. Clinical features of airway malacia in children: a retrospective analysis of 459 patients. Int J Clin Exp Med 2014; 7(9): 3005-12.
[PMID: 25356175]
[10]
Puvabanditsin S, Gengel N, Botti C, et al. 8p 11 Microduplication is associated with neonatal stridor. Mol Syndromol 2019; 9(6): 324-7.
[http://dx.doi.org/10.1159/000494796] [PMID: 30800050]
[11]
Herrera P, Caldarone C, Forte V, et al. The current state of congenital tracheal stenosis. Pediatr Surg Int 2007; 23(11): 1033-44.
[http://dx.doi.org/10.1007/s00383-007-1945-3] [PMID: 17712567]
[12]
Lin S-S, Tzeng B-H, Lee K-R, Smith RJ, Campbell KP, Chen CC. Cav3.2 T-type calcium channel is required for the NFAT-dependent Sox9 expression in tracheal cartilage. Proc Natl Acad Sci USA 2014; 111(19): E1990-8.
[http://dx.doi.org/10.1073/pnas.1323112111] [PMID: 24778262]
[13]
Jacobs IJ, Que J. Genetic and cellular mechanisms of the formation of esophageal atresia and tracheoesophageal fistula. Dis Esophagus 2013; 26(4): 356-8.
[http://dx.doi.org/10.1111/dote.12055] [PMID: 23679023]
[14]
Kause F, Zhang R, Ludwig M, et al. A new autosomal recessive candidate gene for the VATER/VACTERL malformation spectrum. Birth Defects Res 2019.bdr2.1493.
[15]
Mehta AC, Ahmad M, Golish JA, Buonocore E. Congenital anomalies of the lung in the adult. Cleve Clin Q 1983; 50(4): 401-16.
[http://dx.doi.org/10.3949/ccjm.50.4.401] [PMID: 6667546]
[16]
Naidich DP, Zinn WL, Ettenger NA, McCauley DI, Garay SM. Basilar segmental bronchi: thin-section CT evaluation. Radiology 1988; 169(1): 11-6.
[http://dx.doi.org/10.1148/radiology.169.1.3420245] [PMID: 3420245]
[17]
Bartram U, Wirbelauer J, Speer CP. Heterotaxy syndrome -- asplenia and polysplenia as indicators of visceral malposition and complex congenital heart disease. Biol Neonate 2005; 88(4): 278-90.
[http://dx.doi.org/10.1159/000087625] [PMID: 16113522]
[18]
Landing BH, Lawrence TY, Payne VC Jr, Wells TR. Bronchial anatomy in syndromes with abnormal visceral situs, abnormal spleen and congenital heart disease. Am J Cardiol 1971; 28(4): 456-62.
[http://dx.doi.org/10.1016/0002-9149(71)90010-5] [PMID: 5095933]
[19]
Cappuccio G, Rossi A, Fontana P, et al. Bronchial isomerism in a Kabuki syndrome patient with a novel mutation in MLL2 gene. BMC Med Genet 2014; 15(1): 15.
[http://dx.doi.org/10.1186/1471-2350-15-15] [PMID: 24472332]
[20]
Finder JD. Primary bronchomalacia in infants and children. J Pediatr 1997; 130(1): 59-66.
[http://dx.doi.org/10.1016/S0022-3476(97)70311-1] [PMID: 9003852]
[21]
Hysinger EB, Panitch HB. Paediatric Tracheomalacia. Paediatr Respir Rev 2016; 17: 9-15.
[PMID: 25962857]
[22]
Balasubramanian M, Lord H, Levesque S, et al. DDD Study. Chitayat syndrome: hyperphalangism, characteristic facies, hallux valgus and bronchomalacia results from a recurrent c.266A>G p.(Tyr89Cys) variant in the ERF gene. J Med Genet 2017; 54(3): 157-65.
[http://dx.doi.org/10.1136/jmedgenet-2016-104143] [PMID: 27738187]
[23]
Ahel V, Severinski S, Vukas D, Rozmanić V. Primary bronchomalacia and patent ductus arteriosus: Simultaneous surgical correction in an infant. Tex Heart Inst J 1999; 26(3): 215-8.
[PMID: 10524752]
[24]
Gallucci M, di Palmo E, Bertelli L, Camela F, Ricci G, Pession A. A pediatric disease to keep in mind: diagnostic tools and management of bronchiectasis in pediatric age. Ital J Pediatr 2017; 43(1): 117.
[http://dx.doi.org/10.1186/s13052-017-0434-0] [PMID: 29284507]
[25]
Kartagener M. Zur Pathogenese der Bronchiektasien. Beitr Klin Tuberk Spezif Tuberkuloseforsch Springer-Verlag 1933; 83(4): 489-501.
[http://dx.doi.org/10.1007/BF02141468]
[26]
Williams H, Campbell P. Generalized bronchiectasis associated with deficiency of cartilage in the bronchial tree. Arch Dis Child 1960; 35(180): 182-91.
[http://dx.doi.org/10.1136/adc.35.180.182] [PMID: 13844857]
[27]
Davis SD, Ferkol TW, Rosenfeld M, et al. Clinical features of childhood primary ciliary dyskinesia by genotype and ultrastructural phenotype. Am J Respir Crit Care Med 2015; 191(3): 316-24.
[http://dx.doi.org/10.1164/rccm.201409-1672OC] [PMID: 25493340]
[28]
Zariwala MA, Knowles MR, Omran H. Genetic defects in ciliary structure and function. Annu Rev Physiol 2007; 69(1): 423-50.
[http://dx.doi.org/10.1146/annurev.physiol.69.040705.141301] [PMID: 17059358]
[29]
Lucas JS, Barbato A, Collins SA, et al. European Respiratory Society guidelines for the diagnosis of primary ciliary dyskinesia. Eur Respir J 2017; 49(1)1601090
[http://dx.doi.org/10.1183/13993003.01090-2016] [PMID: 27836958]
[30]
Lucas JS, Leigh MW. Diagnosis of primary ciliary dyskinesia: searching for a gold standard. Eur Respir J 2014; 44(6): 1418-22.
[http://dx.doi.org/10.1183/09031936.00175614] [PMID: 25435529]
[31]
Shapiro AJ, Zariwala MA, Ferkol T, et al. Genetic Disorders of Mucociliary Clearance Consortium. Diagnosis, monitoring, and treatment of primary ciliary dyskinesia: PCD foundation consensus recommendations based on state of the art review. Pediatr Pulmonol 2016; 51(2): 115-32.
[http://dx.doi.org/10.1002/ppul.23304] [PMID: 26418604]
[32]
Damseh N, Quercia N, Rumman N, Dell SD, Kim RH. Primary ciliary dyskinesia: mechanisms and management. Appl Clin Genet 2017; 10: 67-74.
[http://dx.doi.org/10.2147/TACG.S127129] [PMID: 29033599]
[33]
Daniels MLA, Noone PG. Genetics, diagnosis, and future treatment strategies for primary ciliary dyskinesia. Expert Opin Orphan Drugs 2015; 3(1): 31-44.
[http://dx.doi.org/10.1517/21678707.2015.989212] [PMID: 26998415]
[34]
Werner C, Onnebrink JG, Omran H. Diagnosis and management of primary ciliary dyskinesia. Cilia 2015; 4(1): 2.
[http://dx.doi.org/10.1186/s13630-014-0011-8] [PMID: 25610612]
[35]
Bukowy-Bieryllo Z, Dabrowski M, Witt M, Zietkiewicz E. Aminoglycoside-stimulated readthrough of premature termination codons in selected genes involved in primary ciliary dyskinesia. RNA Biol 2016; 13(10): 1041-50.
[http://dx.doi.org/10.1080/15476286.2016.1219832] [PMID: 27618201]
[36]
Hayes D Jr, Reynolds SD, Tumin D. Outcomes of lung transplantation for primary ciliary dyskinesia and Kartagener syndrome. J Heart Lung Transplant 2016; 35(11): 1377-8.
[http://dx.doi.org/10.1016/j.healun.2016.08.025] [PMID: 27746084]
[37]
Correia-Pinto J, Gonzaga S, Huang Y, Rottier R. Congenital lung lesions--underlying molecular mechanisms. Semin Pediatr Surg 2010; 19(3): 171-9.
[http://dx.doi.org/10.1053/j.sempedsurg.2010.03.003] [PMID: 20610189]
[38]
Ardini-Poleske ME, Clark RF, Ansong C, et al. LungMAP: The Molecular Atlas of Lung Development Program In: Am J Physiol Cell Mol Physiol. 2017; 313: pp. (5)L733-40.
[39]
Lüdtke TH, Rudat C, Wojahn I, et al. Tbx2 and Tbx3 act downstream of Shh to maintain canonical Wnt signaling during branching morphogenesis of the murine lung. Dev Cell 2016; 39(2): 239-53.
[http://dx.doi.org/10.1016/j.devcel.2016.08.007] [PMID: 27720610]
[40]
Karolak JA, Vincent M, Deutsch G, et al. Complex Compound Inheritance of Lethal Lung Developmental Disorders Due to Disruption of the TBX-FGF Pathway. Am J Hum Genet 2019; 104(2): 213-28.
[http://dx.doi.org/10.1016/j.ajhg.2018.12.010] [PMID: 30639323]
[41]
Chen F, Desai TJ, Qian J, Niederreither K, Lü J, Cardoso WV. Inhibition of Tgf beta signaling by endogenous retinoic acid is essential for primary lung bud induction. Development 2007; 134(16): 2969-79.
[http://dx.doi.org/10.1242/dev.006221] [PMID: 17634193]
[42]
Mendelsohn C, Lohnes D, Décimo D, et al. Function of the retinoic acid receptors (RARs) during development (II). Multiple abnormalities at various stages of organogenesis in RAR double mutants. Development 1994; 120(10): 2749-71.
[PMID: 7607068]
[43]
Bearn JG. The association of sirenomelia with Potter’s syndrome. Arch Dis Child 1960; 35(181): 254-8.
[http://dx.doi.org/10.1136/adc.35.181.254] [PMID: 13688247]
[44]
Bain AD, Beath MM, Flint WF. Sirenomelia and monomelia with renal agenesis and amnion nodosum. Arch Dis Child 1960; 35(181): 250-3.
[http://dx.doi.org/10.1136/adc.35.181.250] [PMID: 13795887]
[45]
Fraga JR, Mirza AM, Reichelderfer TE. Association of pulmonary hypoplasia, renal anomalies, and Potter’s facies. Clin Pediatr (Phila) 1973; 12(3): 150-3.
[http://dx.doi.org/10.1177/000992287301200309] [PMID: 4144828]
[46]
Crowley M. Neonatal respiratory disorders. In: Martin RJ, Richard J, Fanaroff AA, Walsh MC, Eds. Fanaroff and Martin’s neonatalperinatal medicine : diseases of the fetus and infant Volume 2 10th ed. Philadelphia: Elsevier 2015; pp. 1113-36.
[47]
Finegold MJ, Katzew H, Genieser NB, Becker MH. Lung structure in thoracic dystrophy. Am J Dis Child 1971; 122(2): 153-9.
[PMID: 5564158]
[48]
Berrocal T, Madrid C, Novo S, Gutiérrez J, Arjonilla A, Gómez-León N. Congenital anomalies of the tracheobronchial tree, lung, and mediastinum: embryology, radiology, and pathology. Radiographics 2004; 24(1): e17-7.
[http://dx.doi.org/10.1148/rg.e17] [PMID: 14610245]
[49]
Kozenko M, Grynspan D, Oluyomi-Obi T, Sitar D, Elliott AM, Chodirker BN. Potential teratogenic effects of allopurinol: a case report. Am J Med Genet A 2011; 155A(9): 2247-52.
[http://dx.doi.org/10.1002/ajmg.a.34139] [PMID: 21815259]
[50]
Kool H, Mous D, Tibboel D, de Klein A, Rottier RJ. Pulmonary vascular development goes awry in congenital lung abnormalities. Birth Defects Res C Embryo Today 2014; 102(4): 343-58.
[http://dx.doi.org/10.1002/bdrc.21085] [PMID: 25424472]
[51]
Ngo M-LD, Aggarwal A, Knudson JD. Peripheral pulmonary artery stenosis: An unusual case and discussion of genetic associations. Congenit Heart Dis 2014; 9(5): 448-52.
[http://dx.doi.org/10.1111/chd.12198] [PMID: 24965779]
[52]
Griffin N, Mansfield L, Redmond KC, et al. Imaging features of isolated unilateral pulmonary artery agenesis presenting in adulthood: a review of four cases. Clin Radiol 2007; 62(3): 238-44.
[http://dx.doi.org/10.1016/j.crad.2006.10.006] [PMID: 17293217]
[53]
Ten Harkel ADJ, Blom NA, Ottenkamp J. Isolated unilateral absence of a pulmonary artery: a case report and review of the literature. Chest 2002; 122(4): 1471-7.
[http://dx.doi.org/10.1378/chest.122.4.1471] [PMID: 12377882]
[54]
Wasilewska E, Lee EY, Eisenberg RL. Unilateral hyperlucent lung in children. AJR Am J Roentgenol 2012; 198(5) W400-14
[http://dx.doi.org/10.2214/AJR.11.7028] [PMID: 22528920]
[55]
Strenge S, Heinritz W, Zweier C, et al. Pulmonary artery sling and congenital tracheal stenosis in another patient with Mowat-Wilson syndrome. Am J Med Genet A 2007; 143A(13): 1528-30.
[http://dx.doi.org/10.1002/ajmg.a.31801] [PMID: 17567886]
[56]
Remy-Jardin M, Remy J, Mayo J, et al. Vascular anomalies of the lungCT angiography of the chest Philadelphia. Lippincott Williams & Wilkins 2001; pp. 97-114.
[57]
Prosnitz AR, Leopold J, Irons M, Jenkins K, Roberts AE. Pulmonary vein stenosis in patients with Smith-Lemli-Opitz syndrome. Congenit Heart Dis 2017; 12(4): 475-83.
[http://dx.doi.org/10.1111/chd.12471] [PMID: 28719049]
[58]
Lee EY, Boiselle PM, Cleveland RH. Multidetector CT evaluation of congenital lung anomalies. Radiology 2008; 247(3): 632-48.
[http://dx.doi.org/10.1148/radiol.2473062124] [PMID: 18487532]
[59]
Lee EY, Dorkin H, Vargas SO. Congenital pulmonary malformations in pediatric patients: review and update on etiology, classification, and imaging findings. Radiol Clin North Am 2011; 49(5): 921-48.
[http://dx.doi.org/10.1016/j.rcl.2011.06.009] [PMID: 21889015]
[60]
Gossage JR, Kanj G. Pulmonary arteriovenous malformations. A state of the art review. Am J Respir Crit Care Med 1998; 158(2): 643-61.
[http://dx.doi.org/10.1164/ajrccm.158.2.9711041] [PMID: 9700146]
[61]
Rimmer J, Lund VJ. A modified technique for septodermoplasty in hereditary hemorrhagic telangiectasia. Laryngoscope 2014; 124(1): 67-9.
[http://dx.doi.org/10.1002/lary.24303] [PMID: 23832829]
[62]
Govani FS, Shovlin CL. Hereditary haemorrhagic telangiectasia: a clinical and scientific review. Eur J Hum Genet 2009; 17(7): 860-71.
[http://dx.doi.org/10.1038/ejhg.2009.35] [PMID: 19337313]
[63]
Kühnel T, Wirsching K, Wohlgemuth W, Chavan A, Evert K, Vielsmeier V. Hereditary Hemorrhagic Telangiectasia. Otolaryngol Clin North Am 2018; 51(1): 237-54.
[http://dx.doi.org/10.1016/j.otc.2017.09.017] [PMID: 29217066]

© 2024 Bentham Science Publishers | Privacy Policy