Frontometaphyseal dysplasia and keloid formation without FLNA mutations. (21st April 2015)

• Record Type: Journal Article
• Authors: Basart, Hanneke; van de Kar, Annekatrien; Adès, Lesley; Cho, Tae‐Joon; Carter, Erin; Maas, Saskia M.; Wilson, Louise C.; van der Horst, Chantal M. A. M.; Wade, Emma M.; Robertson, Stephen P.; Hennekam, Raoul C.
• Is Part Of: American journal of medical genetics. Volume 167:Number 6(2015:Jun.)
• Page Start: 1215
• Page End: 1222
• Publication Date: 2015-04-21
• Subjects: frontometaphyseal dysplasia -- filamin A -- keloid -- hypertrophic scar -- cleft palate -- Robin sequence -- intellectual disability -- otopalatodigital spectrum disorder; Medical genetics -- Periodicals; 616.14205
• DOI: 10.1002/ajmg.a.37044
• Languages: English
• ISSNs: 1552-4825

Abstract

Abstract : Frontometaphyseal dysplasia (FMD) is a distinctive sclerosing skeletal dysplasia associated with a number of non‐skeletal manifestations including hearing loss, cardiac malformations, and stenosis, particularly of the upper airway and urinary tract. Some, but not all, patients have mutations in FLNA causing the condition. Consonant with the X chromosomal location of FLNA males are generally more severely affected than females. FLNA mutations can be detected in 82% of affected males. We describe seven patients (one male, six females) all of whom have the major clinical and radiological features of FMD, but without detectable mutations in FLNA . The females in our cohort are affected to a similar degree as is usually found in males. In addition, all patients have marked keloid formation at various body sites, including the eye, from an early age. Other features that may indicate a different etiology in these patients are the increased frequency of cleft palate, Robin sequence, tracheal stenosis, and mild intellectual disability, which all occur in three of more patients in the present group. All patients are isolated. We hypothesize that the presently reported patients represent further evidence that phenotypes strongly resembling FMD exist that are not accounted for by mutations in FLNA . Since the frequency of several of the manifestations, their sporadic presentations, and the presence of keloid formation differ from the X‐linked form of this condition we propose de novo autosomal dominant acting mutations in a gene functionally related to FLNA, underpin this disorder. © 2015 Wiley Periodicals, Inc.