Document
Neonatal stridor in familial congenital laryngeal paralysis (Plott syndrome) : a case study in an Omani family.
Identifier
DOI 10.5001/omj.2017.98
Contributors
Prashanth, Gowda Parameshwara., Author
Aguiar, Rodney., Author
Shivalingam, Ganji., Author
Al-Haq, Adeel Ahmed., Author
Publisher
Oman Medical Specialty Board.
Gregorian
2017-11
Language
English
English abstract
Stridor presenting soon after birth due to bilateral abductor vocal cord paralysis (VCP) is rare. We report a family with bilateral VCP affecting four male members in two generations and hence suggesting X-linked recessive inheritance. Severe stridor in the neonatal period requires meticulous airway evaluation, and tracheostomy in 35–70% cases. The current trend is towards conservative management and tracheostomy is avoided unless respiratory distress is severe or life-threatening. Neonatal VCP can be an isolated finding, or it can be familial with or without syndromic features. There are very few reports of non-syndromic familial cases. Unlike the cases reported previously, none of our patients required prolonged intubation or tracheostomy suggesting an excellent prognosis in such cases. This is the first case study of congenital familial non-syndromic VCP reported from the Middle East.
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Category
Journal articles