scholarly journals An appraisal study of donkey in three Northern states of Nigeria

2021 ◽  
Vol 30 (2) ◽  
pp. 203-208
Author(s):  
O. O. J. Bale ◽  
C.A.M. Lakpini ◽  
A. K. Mohammed ◽  
J. T. Amodu ◽  
U. F. Chiezey ◽  
...  

This qualitative study on donkey was conducted in Bauchi, Kano and Kebbi States of Nigeria. The objective of the study was to understand the role, significance and potential areas needing intervention in donkey rearing in the rural setting. The study was also used to obtain first-hand baseline information on the state of knowledge on the donkey in the states surveyed. Sixty two locations were visited comprising 36 from Kebbi, 19 from Bauchi and 17 from Kano States respectively. Rapid Rural Participatory Appraisal (RRPA) technique with check list of questions and farmers' participation was employed in villages/towns randomly selected to cover all the ecological zones in each of the three States. A meeting of one to two hours was organized with the farmers and donkey owners. Observations were made on donkeys at home and in the field. Problems mentioned by respondents included: Colics (Anomari),ulcerative lymphangitis, inflammation of the tongue, interdigital dermatitis, ear sore, fistulous withers, unknown causes of lameness and nervous system disorder called locally as "chinkai chinkai". There were generally poor or no veterinary facilities and services in most of the villages and towns. It was not the farmers practice to take donkeys to clinic for treatment. Mortality was high during the late dry season in most places but also occurred in the rainy season in some places. Areas for further investigations were also highlighted.

2020 ◽  
Vol 18 (2) ◽  
pp. 124-132
Author(s):  
Ibrahim T Ibrahim ◽  
◽  
Suad M Al-Deen ◽  
Ajial S Hassan

2015 ◽  
Vol 86 (11) ◽  
pp. e4.51-e4
Author(s):  
Timothy Lavin ◽  
Sarah Al-Bachari ◽  
David Yunus Gosal

Sensory Neuronopathy (SN) represents a distinct peripheral nervous system disorder associated with degeneration of the Dorsal Root Ganglia. We present our retrospective review of 103 patients with an electro-clinical diagnosis of SN.Average age of onset was 54 yr. Aetiologies included Sjogrens (21%), Probable Inflammatory (16%), Idiopathic (29%), Inherited (20%), Toxic (5%) and paraneoplastic (9%).Of those with inherited SN (n=21); CANVAS syndrome 2/21, mitochrondrial cytopathy 9/21 with 4 confirmed POLG1 mutations, 3/21 presumed HSANIIb, Frederich's Ataxia 1/21 and 6/21 unidentified phenotypes.Clinically, acquired causes commonly presented with pain (62%), asymmetrical/non-length dependent sensory disturbance (91%) as compared to the inherited group who are more likely to present with gait disturbance without prominent sensory symptoms (52%).Of the cohort with presumed inflammatory disease, 29 patients were immunosuppressed with 12 patients responding to a combination of steroids and Mycophenolate. IVIG was not found to be beneficial with no sustained benefit in 7 patients.Paraneoplastic causes (n=9) included Breast (n=2), Neuroendocrine tumours (n=2), Carcinoid (n=2), Bowel (n=1), SCLC (n=1) and unknown primary (n=1) with only 4 Hu positiveConclusionsSensory neuronopathy is clinically and aetiologically pleomorphic. In cases with a suspected inflammatory cause it is worthwhile considering a trial of immunomodulatory treatment.


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