Cleft Lip and/or Palate with Monogenic Autosomal Recessive Transmission in Pyrenees Shepherd Dogs

2009 ◽  
Vol 46 (1) ◽  
pp. 81-88 ◽  
Author(s):  
Cordula Kemp ◽  
Holger Thiele ◽  
Anja Dankof ◽  
Gül Schmidt ◽  
Carola Lauster ◽  
...  

Objective: To document the genetic background of Pyrenees shepherd dogs as it relates to the incidence of cleft lip and/or cleft palate, to describe the phenotype, and to determine possible candidate genes. Design: Pedigree analysis was performed and blood samples were taken from five affected pups, their siblings, and parents. Seven candidate genes were selected and linkage analysis was performed. Further methods used included sequencing and histology. Results: In 37 litters consisting of 163 pups, we found 47 affected pups in a total population of 2104. The male:female ratio was 1:0.96. Affected pups showed isolated cleft lip and/or cleft palate; no attendant disorders have been reported. Despite a high degree of relationship, two affected pups displayed a cleft palate (– H S H –) and a cleft lip with or without cleft palate (L A —) cleft formation. Histology of affected pups showed that the medial edge epithelium remained intact and did not undergo an epithelial-mesenchymal transformation. There was no evidence for linkage between the trait and TGFb3 or Msx1. Subsequent sequencing excluded the coding sequence of Fst as well. Conclusion: Pedigree analysis showed that cleft palate is not genetically distinct from cleft lip with or without cleft palate but is inherited in this breed as a monogenic autosomal recessive trait. Linkage analysis and sequencing excluded TGFb3, Msx1, and Fst as candidate genes. Histology of affected pups showed that the medial edge epithelium is still intact.

2018 ◽  
Vol 26 (10) ◽  
pp. 1441-1450 ◽  
Author(s):  
Brett T Chiquet ◽  
Qiuping Yuan ◽  
Eric C. Swindell ◽  
Lorena Maili ◽  
Robert Plant ◽  
...  

Medicine ◽  
2019 ◽  
Vol 98 (26) ◽  
pp. e16170 ◽  
Author(s):  
Xing Ge ◽  
Jia-Wei Hong ◽  
Jun-Yu Shen ◽  
Zheng Li ◽  
Rui Zhang ◽  
...  

1993 ◽  
Vol 30 (9) ◽  
pp. 773-778 ◽  
Author(s):  
G M Vintiner ◽  
K K Lo ◽  
S E Holder ◽  
R M Winter ◽  
S Malcolm

2010 ◽  
Vol 88 (7) ◽  
pp. 538-545 ◽  
Author(s):  
Adrianna Mostowska ◽  
Kamil K. Hozyasz ◽  
Piotr Wojcicki ◽  
Barbara Biedziak ◽  
Patrycja Paradowska ◽  
...  

2000 ◽  
Vol 37 (4) ◽  
pp. 357-362 ◽  
Author(s):  
Fung Ki Wong ◽  
Catharina Hagberg ◽  
Agneta Karsten ◽  
Ola Larson ◽  
Maria Gustavsson ◽  
...  

2000 ◽  
Vol 37 (4) ◽  
pp. 357-362 ◽  
Author(s):  
Fung Ki Wong ◽  
Catharina Hagberg ◽  
Agneta Karsten ◽  
Ola Larson ◽  
Maria Gustavsson ◽  
...  

2014 ◽  
Vol 2014 ◽  
pp. 1-5
Author(s):  
Meltem Ozdemir-Karatas ◽  
Didem Ozdemir-Ozenen ◽  
P. Suzanne Hart ◽  
Thomas C. Hart

Background.The orofaciodigital syndromes (OFDS) are a heterogeneous group of syndromes that affect the face, oral cavity, and the digits. OFDS type IV (OMIM %258860) is rare and characterized by broad nasal root and tip, orbital hypertelorism or telecanthus, micrognathia, hypoplastic mandible, and low-set ears. Oral symptoms may include cleft lip, cleft or highly arched palate, bifid uvula, cleft or hypoplastic maxillary and mandibular alveolar ridge, oral frenula, lingual hamartoma, and absent or hypoplastic epiglottis. Dental anomalies are common and generally include disturbances in the number of teeth.Case Report.This report presents a six-year-old girl, referred with the chief complaint of missing teeth. She was diagnosed as having OFDS type IV based on clinical findings. Her parents reported three deceased children and two fetuses that had the same phenotype. She was the seventh child of consanguineous parents who were first cousins.Conclusion.This is a very rare syndrome. Many reported OFDS type IV cases have consanguineous parents, consistent with an autosomal recessive trait. Manifestation of cleft palate in the healthy sibling may be mild expression of the disorder or an unrelated isolated cleft.


BMC Genetics ◽  
2016 ◽  
Vol 17 (1) ◽  
Author(s):  
Nurul Syazana Mohamad Shah ◽  
Iman Salahshourifar ◽  
Sarina Sulong ◽  
Wan Azman Wan Sulaiman ◽  
Ahmad Sukari Halim

2019 ◽  
Vol 40 (1) ◽  
pp. 497
Author(s):  
Keylla Helena Nobre Pacifico Pereira ◽  
Caio Henrique Paganini Burini ◽  
Elton Luís Ritir Oliveira ◽  
Lucas Emanuel Ferreira Canuto ◽  
Luiz Eduardo Cruz Dos Santos Correia ◽  
...  

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.


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