Prenatal sonographic diagnosis of Nager acrofacial dysostosis with unilateral upper limb involvement.
نویسندگان
چکیده
Nager acrofacial dysostosis is a rare form of acrofacial dysostosis first described by Nager and de Reynier, 1948. It is characterized by mandibulofacial dysostosis and limb anomalies. Typical craniofacial findings include down-slanting palpebral fissures, malar hypoplasia, micrognathia, abnormalities of the palate including high-arched hard palate, cleft palate or bifid uvula, small, low-set and posteriorly rotated ears, and abnormalities of the external and middle ear. Limb malformations associated with Nager acrofacial dysostosis most often involve the radial aspect of the upper limbs and may result in thumb hypoplasia or aplasia and/or aplasia/hypoplasia of the radius. Findings in a single affected individual are often not symmetrical but both upper limbs are usually involved. Severity can range from mild hypoplasia of the thumb to phocomelia. Radio-ulnar synostosis and abnormalities of the lower limbs have also been reported. Intelligence is typically normal. Congenital bilateral conductive hearing loss, speech difficulties and upper airway obstruction are common secondary to otologic and oral/mandibular abnormalities. A review of reported cases indicates wide variability in manifestations and severity of craniofacial and limb findings (Halal et al., 1983; Hall, 1989; Le Merrer et al., 1989; Danziger et al., 1990; Aylsworth et al., 1991). Cases of Nager acrofacial dysostosis are most often sporadic; however, several cases of autosomal dominant inheritance have been reported (Hall, 1989; Aylsworth et al., 1991). There are also reports of recurrence in children of unaffected parents, suggesting either autosomal recessive inheritance, possible germ line or somatic mosaicism, and, therefore, genetic heterogeneity (Chemke et al., 1988). Diagnosis depends on recognition of the phenotype, most often without a family history. A 23-year-old G2P0010 female presented for second trimester ultrasound at 20 weeks gestation based
منابع مشابه
A Case Report: Nager Acrofacial Dysostosis
Introduction: Nager syndrome is a malformation resulting from problems in the development of the first and second branchial arches and limb buds. The cause of the abnormal development of the pharyngeal arches in Nager syndrome is unknown. It is also unclear why affected individuals have bone abnormalities in their arms and legs. Nager syndrome is thought to have an autosomal recessive inherita...
متن کاملLimbal dermoid in Nager syndrome acrofacial dysostosis: A rare case report.
Nager syndrome, also called preaxial acrofacial dysostosis, comprises two groups of defects involving the limbs and craniofacial region, respectively. This syndrome is rare and only 70 cases have been reported in the literature. The exact cause of this syndrome is unknown, but there is indication that it is genetically based. Ocular manifestations of this syndrome include widely separated downw...
متن کاملA novel malformation complex of bilateral and symmetric preaxial radial ray-thumb aplasia and lower limb defects with minimal facial dysmorphic features: a case report and literature review
INTRODUCTION Radial hemimelia is a congenital abnormality characterised by the partial or complete absence of the radius. The longitudinal hemimelia indicates the absence of one or more bones along the preaxial (medial) or postaxial (lateral) side of the limb. Preaxial limb defects occurred more frequently with a combination of microtia, esophageal atresia, anorectal atresia, heart defects, uni...
متن کاملAutosomal recessive inheritance of Nager acrofacial dysostosis.
Nager acrofacial dysostosis is a variant of mandibulofacial dysostosis with severe micrognathia, malar hypoplasia, and radial limb defects. Most cases are sporadic, but autosomal recessive inheritance has been suggested. A family is reported in which two sibs are affected by this syndrome, presenting further evidence for autosomal recessive inheritance. The recognition of this syndrome as a dis...
متن کاملAcrofacial dysostosis of Nager and ocular abnormalities.
Acrofacial dysostosis of Nager is a little known hereditary syndrome in which the findings of mandibulofacial dysostosis are associated with defects of the limbs. The present case showed other abnormalities including the Stilling-Turk-Duane syndrome, conductive deafness and ptosis of the transverse colon.
متن کاملذخیره در منابع من
با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید
برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید
ثبت ناماگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید
ورودعنوان ژورنال:
- Prenatal diagnosis
دوره 28 10 شماره
صفحات -
تاریخ انتشار 2008