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Prenatal Diagnosis of Acromelic Frontonasal Dysostosis.

ABSTRACT: Acromelic frontonasal dysostosis (AFND; MIM #603671) is a rare autosomal dominant genetic disorder caused by a heterozygous mutation in the ZSWIM6 (KIAA1577) gene located at chromosome 5q12.1. It is phenotypically characterized by frontonasal malformation with hypertelorism, telecanthus, nasal clefting or bifid nasal tip, wide fontanels and sutures, brachycephaly, and cleft palate. The patients also present with central nervous system malformations such as encephalocele, agenesis of the corpus callosum, or interhemispheric lipoma. Limb malformations can also be found, including preaxial polydactyly of the feet and sometimes postaxial polydactyly of the hands, talipes equinovarus, or tibia malformations. Here, we present a case of early prenatal diagnosis of AFND with ultrasound and necropsy images which show the phenotypic findings of this syndrome.

SUBMITTER: Martinez-Payo C

PROVIDER: S-EPMC7983669 | biostudies-literature | 2021 Mar

REPOSITORIES: biostudies-literature

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Prenatal Diagnosis of Acromelic Frontonasal Dysostosis.

Martínez-Payo Cristina C García-Santiago Fe Amalia FA Heath Karen E KE Gavin Eduardo E Mansilla-Aparicio Elena E

Molecular syndromology 20201215 1

Acromelic frontonasal dysostosis (AFND; MIM #603671) is a rare autosomal dominant genetic disorder caused by a heterozygous mutation in the <i>ZSWIM6</i> (<i>KIAA1577</i>) gene located at chromosome 5q12.1. It is phenotypically characterized by frontonasal malformation with hypertelorism, telecanthus, nasal clefting or bifid nasal tip, wide fontanels and sutures, brachycephaly, and cleft palate. The patients also present with central nervous system malformations such as encephalocele, agenesis o ...[more]

PMID: 33776626

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