Achondroplasia: a case report and the review of the basics

dc.date.accessioned2020-11-18T10:05:08Z
dc.date.available2020-11-18T10:05:08Z
dc.date.issued2020-07
dc.description.abstractThe achondroplasia is a variant of short-limbed dwarfism. The word achondroplasia literally means without cartilage formation. However, in achondroplasia the problem is not in formation of cartilage but, in its conversion to bone (i.e. ossification). This deficient ossification is particularly seen in the long bones of arm and leg. The characteristic external appearance of people born with achondroplasia is short stature. The average height of an adult male with achondroplasia is 131 centimetres (4 feet, 4 inches), and the average height for adult females is 124 centimetres (4 feet, 1 inch). The trunk is of average size but the leg and upper arm is of short length. It is because the femur and humerus are relatively shorter in length. The range of movement at elbow is limited. The head is enlarged called macrocephaly and is with a prominent forehead. People with Achondroplasia are generally of normal intelligence. They have bowed legs and abnormal curvature of spine giving rise to lordosis or kyphosis. They may develop spinal stenosis, which is associated with pain, tingling and weakness in leg. This may cause difficulty in walking. The other health problems associated with Achondroplasia are episodes of apnoea, obesity and recurrent ear infection. The purpose of this study is to evaluate the cardinal phenotypic features in patient of Achondroplasia. It is also to assess the body physique, anthropometric measurements and to study the typical radiological signs in such patients as the main tool of diagnosis.en_US
dc.identifier.affiliationsDepartment of Surgery, SBRKM Government Medical College, Jagdalpur (Bastar), Chhattisgarh, Indiaen_US
dc.identifier.citationAgrawal Sujan Narayan. Achondroplasia: a case report and the review of the basics. International Surgery Journal. 2020 Jul; 7(7): 2420-2424en_US
dc.identifier.issn2349-3305
dc.identifier.issn2349-2902
dc.identifier.placeIndiaen_US
dc.identifier.urihttps://imsear.searo.who.int/handle/123456789/213201
dc.languageenen_US
dc.publisherMedip Academyen_US
dc.relation.issuenumber7en_US
dc.relation.volume7en_US
dc.source.urihttps://dx.doi.org/10.18203/2349-2902.isj20202862en_US
dc.subjectAchondroplasiaen_US
dc.subjectFibroblast growth factor receptor 3en_US
dc.subjectRhizomeliaen_US
dc.subjectSkeletal dysplasiaen_US
dc.titleAchondroplasia: a case report and the review of the basicsen_US
dc.typeJournal Articleen_US
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