Dear Sir,We read an interesting case report by Ray and Jain.[1] The eminent authors have reported a case of Guillain–Barre Syndrome (GBS) presenting as bulbar palsy plus syndrome. Here, we would like to share our experience and views:Cranial nerve involvement is said to be rare (5%), especially in children by the authors[1] and supported by another reference.[2] We in a prospective study of 61 patients in the age range of 8–78 years, found bulbar palsy in 46.2%, facial palsy in 46%, tongue weakness in 10%, unilateral facial palsy in (3 patients) 5%, ophthalmoplegia in 6.4%, and sensorineural deafness (eighth cranial nerve involvement) in 1 patient.[3] Our observations are almost similar to the earlier text references[4]The authors have said that unilateral facial palsy in GBS is extremely rare, especially in children. We in our study which also included pediatric population found unilateral facial palsy in (three patients) 5% of the patients[3]The present study also concluded that there is a correlation between cranial nerve palsy and severity of GBS, and bulbar palsy is an indicator of respiratory involvement. Careful search of the cranial nerve involvement may yield more and more cranial neuropathies[3]As bulbar involvement is an indicator of impending respiratory involvement, the index case of the eminent authors was lucky enough not have such complication. One reason may be that the patient’s illness stabilized after initial progression for 4 days.