PRUNE BELLY SYNDROME- CASE REPORT
Keywords:
Prune belly syndrome, Congenital abnormalities, Abdominal wall, CryptorchidismAbstract
Prune Belly Syndrome (SPB) is characterized by symptoms that are organized in a triad based on the absence, deficiency or congenital hypoplasia of all abdominal musculature, as well as changes in the urinary tract accompanied by bilateral cryptorchidism. The objective of this study was to report a clinical case of this severe syndrome and to present a brief Physiotherapeutic care protocol. The reported case is of a 3-year-old male patient with bilateral cryptorchidism, malformation of the abdominal musculature and respiratory difficulty using tracheostomy and nasoenteral probe, was investigated at the Sena Aires Science and Education Faculty in Valparaiso de Goiás, where was submitted to a physiotherapeutic protocol. Because it is a serious syndrome, it is necessary to have an effective diagnosis for a rapid physiotherapeutic intervention, since it will be possible to know the limitations of these patients and to provide effective care with the objective of improving the quality of life and its insertion in society, promoting the well-being of the patient. child, besides serving as a guide for new research in the area, especially those with little evidence.
References
Castillo Manrique S, Castillo Maldonado S; Spagnoli N. Medicina (Guayaquil). 2010; 16(1): 59-63.
Gonçalves GS. Souza GD, Queiros LR, Costa VSF. Síndrome de Prune Belly: relato de caso. Rev Med Saude Brasilia 2013; 2(3):125‐32.
Castilho-Weinert LV, Forti-Bellani C. Fisioterapia em Neuropediatria. São Paulo: Omnipax; 2011.
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