Abstract
Congenital defects can cause changes in the normal function or morphology of organs, thus contributing to neonatal mortality. Malformations in dogs occur as a result of genetic factors or by the action of teratogenic agents during pregnancy. Genetic defects can be inherited from one or both parents. These defects are more common in purebred puppies or can even be the result of consanguinity. Teratogenic agents, such as toxins, drugs, infectious diseases, mechanical influences, and irradiation, may affect the litters during gestational development. Hypoplasia of ribs has been described in human newborns. It is a rare and lethal malformation of autosomal recessive inheritance that prevents thoracic expansion and reduces pulmonary compliance, causing respiratory failure. A pregnant bitch of undefined breed was submitted to caesarean section. At birth, a neonate exhibited respiratory distress, and the palpation of the thorax indicated absence of ribs. In addition, the newborn had cleft palate and cleft lip, which led to perform the euthanasia of the animal. Post-mortem examination indicated hypoplasia of ribs and unilateral renal agenesis. As in the canine neonate, hypoplasia of ribs in human newborns is also associated with other malformations, such as cleft lip, cleft palate, and urogenital defects. The present report describes the first case of hypoplasia of ribs associated with other malformations in a canine neonate, the cause being possibly related to a genetic hereditary factor.References
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DAGONEAU, N.; GOULET, M.; GENEVIÈVE, D.; SZNAJER, Y.; MARTINOVIC, J.; SMITHSON, S.; HUBER, C.; BAUJAT, G.; FLORI, E.; TECCO, L.; CAVALCANTI, D.; DELEZOIDE, A. L.; SERRE, V.; LE MERRER, M.; MUNNICH, A.; CORMIER-DAIRE, V. DYNC2H1 mutations cause asphyxiating thoracic dystrophy and short rib-polydactyly syndrome, type III. American Journal of Human Genetics, Houston, v.84, n. 5, p. 706-711, 2009.
DUONG, A.; STEINMAUS, C.; MC-HALE, C. M.; VAUGHAN, C. P.; ZHANG, L. Reproductive and developmental toxicity of formaldehyde: a systematic review. Mutation Research, Amsterdam, v. 728, n. 3, p. 118-138, 2011.
FALCONER, D. S.; MACKAY, T. F. C. Introduction to quantitative genetics. 4th ed. Harlow: Longman Group Limited, 1996. 480 p.
FUJITA, A.; TSUBOI, M.; UCHIDA, K.; NISHIMURA, R. Complex malformations of the urogenital tract in a female dog: gartner duct cyst, ipsilateral renal agenesis, and ipsilateral hydrometra. Japanese Journal of Veterinary Research, Sapporo, v. 64, n. 2, p. 147-152, 2016.
GILL, M. A. Perinatal and late neonatal mortality in the dog. 2001. Thesis (Doctor of Philosophy) -University of Sydney, New South Wales.
GOUGH, A.; THOMAS, A. Breed predispositions to disease in dog and cats. 2th ed. Hoboken: Wiley-Blackwell, 2011. 352 p.
HOSKINS, J. D. Veterinary pediatrics: dogs and cats from birth to six months. 3th ed. Philadelphia: Saunders, 2001. 594 p.
LOURENÇO, M. L. G. Cuidados com neonatos e filhotes. In: JERICÓ, M. M.; KOGIKA, M. M.; ANDRADE NETO, J. P. de. (Ed.). Tratado de medicina interna de cães e gatos. Rio de Janeiro: Roca, 2015. p. 363-675.
PETERSON, M. E.; KUTZLER, M. A. Small animal pediatrics. Saint Louis: Elsevier, 2011. 448 p.
SCHOENEBECK, J. J.; OSTRANDER, E. A. Insights into morphology and disease from the dog genome Project. Annual Review of Cell Developmental Biology, Palo Alto, v. 30, n. 1, p. 535-560, 2014.
VRIES, J.; YNTEMA, J. L.; VAN DIE, C. E.; CRAMA, N.; CORNELISSEN, E. A. M.; HAMEL, B. C. J. Jeune syndrome: description of 13 cases and a proposal for follow-up protocol. European Journal of Pediatrics, Berlim, v. 169, n. 1, p. 77-88, 2010.

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