SciELO - Scientific Electronic Library Online

 
vol.21 issue83Hypoxemia as the only manifestation of structural hemoglobinopathyCongenital drusen in the child, differential diagnosis with papilledema author indexsubject indexarticles search
Home Pagealphabetic serial listing  

Services on Demand

Journal

Article

Indicators

Related links

  • On index processCited by Google
  • Have no similar articlesSimilars in SciELO
  • On index processSimilars in Google

Share


Pediatría Atención Primaria

Print version ISSN 1139-7632

Abstract

RUIZ GUZMAN, Luis et al. Ankyloglossia inheritance: like father, like son. Rev Pediatr Aten Primaria [online]. 2019, vol.21, n.83, pp.e129-e135.  Epub Dec 09, 2019. ISSN 1139-7632.

The pathogenesis of tongue tie and the major or minor expression of the genotype that causes it are not known because it can occur with inheritances X-linked dominant or, in some cases, recessive. Four families with tongue tie in different generations, accompanying infants with breastfeeding problems are presented. In all cases there was a lack of prior knowledge of this situation in patients and family members.

In our medical office, 326 sibling groups were attended. In 133 of them, no frenectomy was performed, in 96 groups one of the brothers underwent surgery, in 91 the two brothers were operated and in 6, three brothers. Prevalence in siblings of 44.9% was found.

The underdiagnosis of ankyloglossia is conditioned by the unawareness of some consequences of this pathology: dental malposition, alterations of the spine, speech disorders, respiratory problems and apnea, among others. Large samples are needed to study the transmission mechanisms and clarify the pathogenesis of this inherited malformation, which affects more than 10% of the population.

Keywords : Ankyloglossia; Lingual frenulum; Inheritance patterns.

        · abstract in Spanish     · text in Spanish     · Spanish ( pdf )