Castori, Marco ORCID: 0000-0002-6069-0993, Pascolini, Giulia ORCID: 0000-0002-2440-7441, Parisi, Valentina, Sana, Maria Elena, Novelli, Antonio ORCID: 0000-0002-9037-4297, Nuernberg, Peter, Iascone, Maria and Grammatico, Paola (2015). Microcephaly, Ectodermal Dysplasia, Multiple Skeletal Anomalies, and Distinctive Facial Appearance: Delineation of Cerebro-Dermato-Osseous-Dysplasia. Am. J. Med. Genet. A, 167 (4). S. 842 - 852. HOBOKEN: WILEY-BLACKWELL. ISSN 1552-4833

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Abstract

In 1980, a novel multiple malformation syndrome has been described in a 17-year-old woman with micro- and turricephaly, intellectual disability, distinctive facial appearance, congenital atrichia, and multiple skeletal anomalies mainly affecting the limbs. Four further sporadic patients and a couple of affected sibs are also reported with a broad clinical variability. Here, we describe a 4-year-old girl strikingly resembling the original report. Phenotype comparison identified a recurrent pattern of multisystem features involving the central nervous system, and skin and bones in five sporadic patients (including ours), while the two sibs and a further sporadic case show significant phenotypic divergence. Marked clinical variability within the same entity versus syndrome splitting is discussed and the term cerebro-dermato-osseous dysplasia is introduced to define this condition. (c) 2015 Wiley Periodicals, Inc.

Item Type: Journal Article
Creators:
CreatorsEmailORCIDORCID Put Code
Castori, MarcoUNSPECIFIEDorcid.org/0000-0002-6069-0993UNSPECIFIED
Pascolini, GiuliaUNSPECIFIEDorcid.org/0000-0002-2440-7441UNSPECIFIED
Parisi, ValentinaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Sana, Maria ElenaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Novelli, AntonioUNSPECIFIEDorcid.org/0000-0002-9037-4297UNSPECIFIED
Nuernberg, PeterUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Iascone, MariaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
Grammatico, PaolaUNSPECIFIEDUNSPECIFIEDUNSPECIFIED
URN: urn:nbn:de:hbz:38-408410
DOI: 10.1002/ajmg.a.36983
Journal or Publication Title: Am. J. Med. Genet. A
Volume: 167
Number: 4
Page Range: S. 842 - 852
Date: 2015
Publisher: WILEY-BLACKWELL
Place of Publication: HOBOKEN
ISSN: 1552-4833
Language: English
Faculty: Unspecified
Divisions: Unspecified
Subjects: no entry
Uncontrolled Keywords:
KeywordsLanguage
MENTAL-RETARDATION; ODONTOTRICHOMELIC SYNDROME; TETRAMELIC DEFICIENCIES; CLEFT LIP/PALATE; SHORT STATURE; MUTATIONS; ALOPECIA; PHENOTYPE; PVRL1Multiple languages
Genetics & HeredityMultiple languages
URI: http://kups.ub.uni-koeln.de/id/eprint/40841

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