Severe cervical kyphosis in osteopathia striata with cranial sclerosis: case report

2001 ◽  
Vol 31 (9) ◽  
pp. 659-662 ◽  
Author(s):  
T. Kondoh ◽  
Muneyoshi Yoshinaga ◽  
Tadashi Matsumoto ◽  
Toshimitsu Takayanagi ◽  
Masataka Uetani ◽  
...  
Keyword(s):  
Case Report ◽  
Cervical Kyphosis ◽  
Osteopathia Striata ◽  
Cranial Sclerosis

Dental Findings in a Child with Osteopathia Striata with Cranial Sclerosis (OS-CS): A Case Report

2013 ◽  
Vol 37 (4) ◽  
pp. 411-413
Author(s):  
M Nishiguchi ◽  
K Satoh ◽  
Y Kamasaki ◽  
T Hoshino ◽  
T Fujiwara
Keyword(s):  
Case Report ◽  
Early Stage ◽  
Permanent Teeth ◽  
Dental Anomalies ◽  
Osteopathia Striata ◽  
Dental Management ◽  
Cranial Sclerosis ◽  
Planning Treatment ◽  
Delayed Eruption ◽  
Oral Abnormalities

The dental management of an 8-year-old girl with osteopathia striata with cranial sclerosis (OS-CS) is described. The girl presented with various oral abnormalities. The aim of this case report was to describe in detail the dental findings in a patient with OC-CS and the precautions to be taken when planning treatment. In the present case, many dental anomalies, such as delayed eruption of the permanent teeth, obliteration of the dental pulp, short roots, fused roots and taurodontism, were detected. In patients with OS-CS, routine dental care from an early stage is recommended to manage this anomaly properly.

Osteopathia striata with cranial sclerosis (OSCS): review of the literature and case report demonstrating challenges of spinal fusion after trauma

2016 ◽  
Vol 158 (6) ◽  
pp. 1115-1120 ◽  
Author(s):  
Gennadiy A. Katsevman ◽  
Ryan C. Turner ◽  
Brandon P. Lucke-Wold ◽  
Cara L. Sedney ◽  
Sanjay Bhatia
Keyword(s):  
Case Report ◽  
Spinal Fusion ◽  
Review Of The Literature ◽  
Osteopathia Striata ◽  
Cranial Sclerosis

Cranial Sclerosis with Striated Bone Disease (Osteopathia Striata)

1986 ◽  
Vol 198 (05) ◽  
pp. 418-424 ◽  
Author(s):  
H. Piechowiak ◽  
F. Goebel ◽  
U. Hirche ◽  
R. Tyrell
Keyword(s):  
Bone Disease ◽  
Osteopathia Striata ◽  
Cranial Sclerosis

First female prenatal case of osteopathia striata with cranial sclerosis in a fetus carrying a de-novo 1.9 Mbp interstitial deletion at Xq11.1q11.2

2017 ◽  
Vol 26 (4) ◽  
pp. 231-234
Author(s):  
Marie-Laure Vuillaume ◽  
Anna-Gaelle Valard ◽  
Nada Houcinat ◽  
Julie Bouron ◽  
Cécile Boucher ◽  
...  
Keyword(s):  
De Novo ◽  
Interstitial Deletion ◽  
Osteopathia Striata ◽  
Cranial Sclerosis

scholarly journals Prenatal Diagnosis of Osteopathia Striata with Cranial Sclerosis in a Male Fetus with a ~330kb Deletion of Xq11.1 Involving the WTX Gene

2013 ◽  
Vol 1 (1) ◽  
pp. 33-36 ◽  
Author(s):  
Patrick L. Wilson ◽  
Ashley Davis ◽  
Jean Ricci Goodman ◽  
Lauren Notley ◽  
Shibo Li ◽  
...  
Keyword(s):  
Prenatal Diagnosis ◽  
Male Fetus ◽  
Osteopathia Striata ◽  
Cranial Sclerosis

Whole Exome Sequencing Provides the Correct Diagnosis in a Case of Osteopathia Striata with Cranial Sclerosis: Case Report of a Novel Frameshift Mutation in AMER1

2020 ◽  
Author(s):  
José María García-Aznar ◽  
Noelia Ramírez ◽  
David De Uña ◽  
Elisa Santiago ◽  
Lorenzo Monserrat
Keyword(s):  
Exome Sequencing ◽  
Whole Exome Sequencing ◽  
Target Genes ◽  
Correct Diagnosis ◽  
Sotos Syndrome ◽  
Pathogenic Variants ◽  
Osteopathia Striata ◽  
Whole Exome ◽  
Cranial Sclerosis ◽  
Extended Analysis

AbstractThe diagnosis of rare diseases with multisystem manifestations can constitute a difficult process that delays the determination of the underlying cause. Whole exome sequencing (WES) provides a suitable option to examine multiple target genes associated with several disorders that display common features. In this study, we report the case of a female patient suspected of having Sotos syndrome. Screening for the initially selected genes, considering Sotos syndrome and Sotos-like disorders, did not identify any pathogenic variants that could explain the phenotype. The extended analysis, which considered all genes in the exome associated with features consistent with those shown by the studied patient, revealed a novel frameshift variant in the AMER1 gene, responsible for osteopathia striata with cranial sclerosis. WES analysis and an updated revision of previously reported disease-causing mutations, proved useful to reach an accurate diagnosis and guide further examination to identify critical abnormalities.

Osteopathia striata with cranial sclerosis and developmental delay in a male with a mosaic deletion in chromosome region Xq11.2

2012 ◽  
Vol 158A (11) ◽  
pp. 2946-2952 ◽  
Author(s):  
Sébastien Chénier ◽  
Abdul Noor ◽  
Lucie Dupuis ◽  
Dimitri J Stavropoulos ◽  
Roberto Mendoza-Londono
Keyword(s):  
Developmental Delay ◽  
Chromosome Region ◽  
Osteopathia Striata ◽  
Cranial Sclerosis
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