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1.
Eur J Pediatr ; 179(8): 1191-1195, 2020 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-32506218

RESUMO

The frenotomy or surgical release of the lingual frenulum is performed with increasing frequency. Restricted tongue mobility, ankyloglossia, is the main indication for this procedure. This clinical diagnosis is often used as synonym for tongue-tie which is blamed for many feeding difficulties resulting in an increase in performed frenotomies. Until recently, little was known about the anatomical structure and normal variation of the tongue-tie. Different grading systems have been developed. Some are exclusively based on appearance of the tongue-tie; others also include functional elements. There is, however, no established relation between the tongue-tie score and the observed feeding problems or outcomes following frenotomy. Therefore, caution is warranted before submitting babies to this procedure.Conclusion: This narrative review aims to give an overview of current knowledge and concerns regarding the tongue-tie, which need to be considered before referral for a frenotomy. What is Known: • The presence of a tongue-tie is associated with a higher frequency of breastfeeding problems. • Hence, frenotomy is advocated and increasingly performed in infants with breastfeeding problems. Current tongue-tie classifications do not allow to predict breastfeeding problems. What is New: • New anatomy insights caution for possible complications resulting from this seemingly innocent practice of frenotomy. • Frenotomy should only be performed after multidisciplinary evaluation of feeding problems, following exclusion and remediation of other causative factors.


Assuntos
Anquiloglossia/cirurgia , Aleitamento Materno , Freio Lingual/cirurgia , Complicações Pós-Operatórias , Anquiloglossia/diagnóstico , Humanos , Lactente , Recém-Nascido , Resultado do Tratamento
2.
Am J Med Genet A ; 173(11): 3104-3108, 2017 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-28884947

RESUMO

We present a 4-year-old girl with delayed neuromotor development, short stature of prenatal onset, and specific behavioral and craniofacial features harboring an intragenic deletion in the ARID2 gene. The phenotype confirmed the major features of the recently described ARID2-related intellectual disability syndrome. However, our patient showed overlapping features with Nicolaides-Baraitser syndrome and Coffin-Siris syndrome, providing further arguments to reclassify these disorders as "SWI/SNF-related intellectual disability syndromes."


Assuntos
Proteínas Cromossômicas não Histona/genética , Deficiência Intelectual/genética , Transtornos Motores/genética , Fatores de Transcrição/genética , Anormalidades Múltiplas/diagnóstico , Anormalidades Múltiplas/genética , Anormalidades Múltiplas/patologia , Pré-Escolar , Face/anormalidades , Face/patologia , Fácies , Feminino , Deformidades Congênitas do Pé/diagnóstico , Deformidades Congênitas do Pé/genética , Deformidades Congênitas do Pé/patologia , Predisposição Genética para Doença , Deformidades Congênitas da Mão/diagnóstico , Deformidades Congênitas da Mão/genética , Deformidades Congênitas da Mão/patologia , Humanos , Hipotricose/diagnóstico , Hipotricose/genética , Hipotricose/patologia , Deficiência Intelectual/diagnóstico , Deficiência Intelectual/patologia , Deficiência Intelectual/fisiopatologia , Micrognatismo/diagnóstico , Micrognatismo/genética , Micrognatismo/patologia , Transtornos Motores/fisiopatologia , Pescoço/anormalidades , Pescoço/patologia
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