2.Acro-dermato-ungual-lacrimal-tooth syndrome: case report.
Jian YANG ; Hong-juan ZHANG ; Wen-lin YANG ; Guang-sheng CHEN ; Zhi-wei TANG ; Shuang CHEN ; Wen-hong YE
Chinese Medical Journal 2007;120(9):851-853
Adult
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Ectodermal Dysplasia
;
genetics
;
pathology
;
Female
;
Fingers
;
abnormalities
;
Humans
;
Nasolacrimal Duct
;
abnormalities
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Syndrome
;
Tooth Abnormalities
;
pathology
4.A de novo GJA1 mutation identified by whole-exome sequencing in a patient with oculodentodigital dysplasia.
Hui ZENG ; Li XIE ; Mi TANG ; Yifeng YANG ; Zhiping TAN
Chinese Journal of Medical Genetics 2018;35(2):268-271
OBJECTIVETo explore the genetic basis for a patient with oculodentodigital dysplasia.
METHODSGenomic DNA was extracted from peripheral blood samples from the patient and his parents. Whole-exome sequencing was carried out for the trio family. Suspected mutation was verified by Sanger sequencing.
RESULTSA de novo c.412G>A mutation of the GJA1 gene was identified in the patient, which was validated by Sanger sequencing.
CONCLUSIONThe c.412G>A mutation of the GJA1 gene probably underlies the disease in the patient.
Adult ; Connexin 43 ; genetics ; Craniofacial Abnormalities ; genetics ; Exome ; Eye Abnormalities ; genetics ; Foot Deformities, Congenital ; genetics ; Humans ; Male ; Mutation ; Sequence Analysis, DNA ; Syndactyly ; genetics ; Tooth Abnormalities ; genetics
5.Dental anomalies in first-degree relatives of transposed canine probands.
Adriana BARTOLO ; Neville CALLEJA ; Fraser MCDONALD ; Simon CAMILLERI
International Journal of Oral Science 2015;7(3):169-173
The aim of this study was to investigate and compare the inheritance pattern and prevalence of inheritable dental anomalies in a sample of patients with maxillary canine-first premolar transposition and their first-degree relatives with a sample of palatally displaced canine families. Thirty-five consecutive maxillary canine-first premolar transposition probands and 111 first-degree relatives were matched to 35 consecutive palatally displaced canine probands and 115 first-degree relatives. These were assessed for palatally displaced canines and incisor-premolar hypodontia. Parental age at birth of the proband was also noted. The results revealed that (i) there is no difference in the overall prevalence of palatally displaced canine or incisor-premolar hypodontia between the groups of relatives; (ii) first-degree relatives of bilateral palatally displaced canine probands have a higher prevalence of palatally displaced canine and incisor-premolar hypodontia than those with unilateral palatally displaced canine; and (iii) maternal age at birth of the maxillary canine-first premolar transposition probands was significantly higher than that of the palatally displaced canine probands. The results suggest that maxillary canine-first premolar transposition and palatally displaced canine are unlikely to be different genetic entities and also indicate environmental or epigenetic influences on dental development.
Cuspid
;
abnormalities
;
diagnostic imaging
;
Family
;
Humans
;
Radiography, Panoramic
;
Tooth Abnormalities
;
etiology
;
genetics
6.Analysis of three patients with KBG syndrome and epileptic seizures due to variants of ANKRD11 gene.
Chao LIU ; Xianhui REN ; Luojun WANG ; Zihan WEI ; Mi CAO ; Guoyan LI ; Zhenyu WU ; Yanchun DENG
Chinese Journal of Medical Genetics 2022;39(5):479-483
OBJECTIVE:
To summarize the clinical phenotype and genotypic characteristics of 3 patients with KBG syndrome and epileptic seizure.
METHODS:
Clinical data of the patients were collected. Family-trio whole exon sequencing (WES) was carried out. Candidate variants were verified by Sanger sequencing.
RESULTS:
Patients 1 and 2 were boys, and patient 3 was an adult woman. All patients had epileptic seizures and mental deficiency. Their facial features included triangular face, low hair line, hypertelorism, large forward leaning auricles, broad nasal bridge, upturned nostrils, long philtrum, arched upper lip, and macrodontia. The two boys also had bilateral Simian creases. WES revealed that the three patients all harbored heterozygous de novo frameshift variants in exon 9 of the ANKRD11 gene including c.2948delG (p.Ser983Metfs*335), c.5397_c.5398insC (p.Glu1800Argfs*150) and c.1180_c.1184delAATAA (p.Asn394Hisfs*42). So far 291 patients with ANKRD11 gene variants or 16q24.3 microdeletions were reported, with over 75% being de novo mutations.
CONCLUSION
Above findings have enriched the spectrum of ANKRD11 gene mutations underlying KBG syndrome. WES is helpful for the early diagnosis of KBG, and provided reference for genetic counseling of this disease.
Abnormalities, Multiple/genetics*
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Bone Diseases, Developmental/genetics*
;
Epilepsy/genetics*
;
Facies
;
Humans
;
Intellectual Disability/genetics*
;
Phenotype
;
Repressor Proteins/genetics*
;
Seizures/genetics*
;
Tooth Abnormalities/genetics*
7.Clinical and genetic analysis of three children with KBG syndrome due to novel variants of ANKRD11 gene.
Li WANG ; Jingjing LI ; Jinghan XU ; Yanlei XU ; Junbo WANG ; Yin FENG ; Xiangdong KONG
Chinese Journal of Medical Genetics 2023;40(1):1-6
OBJECTIVE:
To explore the clinical and genetic characteristics of three children with KBG syndrome.
METHODS:
Clinical data of the three children from two families who have presented at the First Affiliated Hospital of Zhengzhou University between October 2019 and September 2020 and their family members were collected. Trio-whole exome sequencing (trio-WES) and Sanger sequencing were carried out.
RESULTS:
All children had feeding difficulties, congenital heart defects and facial dysmorphism. The sib- pair from family 1 was found to harbor a novel de novo heterozygous c.6270delT (p.Q2091Rfs*84) variant of the ANKRD11 gene, whilst the child from family 2 was found to harbor a novel heterozygous c.6858delC (p.D2286Efs*51) variant of the ANKRD11 gene, which was inherited from his mother who had a mild clinical phenotype.
CONCLUSION
The heterozygous frameshift variants of the ANKRD11 gene probably underlay the disease in the three children. Above findings have enriched the spectrum of the ANKRD11 gene variants.
Female
;
Child
;
Humans
;
Abnormalities, Multiple/genetics*
;
Intellectual Disability/genetics*
;
Bone Diseases, Developmental/genetics*
;
Tooth Abnormalities/genetics*
;
Facies
;
Repressor Proteins/genetics*
;
Mothers
;
Mutation
8.Gender difference in clinical manifestations of KBG syndrome due to variants of ANKRD11 gene.
Yuyao YANG ; Pengqiang WEN ; Zhe SU ; Li WANG ; Xiu ZHAO
Chinese Journal of Medical Genetics 2021;38(7):663-666
OBJECTIVE:
To explore gender difference in the clinical manifestations of two children with Keishi-Bukuryo-Gan syndrome (KBGS).
METHODS:
Clinical manifestations of the two children were reviewed. Genetic testing was carried out through next generation sequencing (NGS). Treatment was summarized, and the prognosis was followed up.
RESULTS:
Both children showed particular appearance including megatooth, abnormal hair distribution, hands' abnormality and language development delay. NGS revealed that both children have carried pathogenic variants of the ANKRD11 gene (c.1903_1907del and c.4911delT), which resulted in shifting of amino acid sequences starting from the Lysine and Proline at positions 635 and 1638, respectively. The female patient exhibited central precocious puberty. Her height has increased by 13 cm, and sex characteristics has retracted after treatment with leuprorelin for 23 months and recombinant human growth hormone for 1 month.
CONCLUSION
Comparison of the two cases with different genders and summary of previously reported cases found that male KBGS patients have more obvious dysmorphisms such as triangular face, synophrys, ocular hypertelorism and vertebral body abnormality, with higher morbidity of epilepsy, mental retardation, autism, congenital heart disease, immune thrombocytopenia and other complications. KBGS is an autosomal dominant disease featuring more evident peculiar appearance and global development delay. Male patients often have multi-system involvement, and multidisciplinary cooperation is required for early recognition of particular features in order to improve the prognosis.
Abnormalities, Multiple
;
Bone Diseases, Developmental
;
Child
;
Facies
;
Female
;
Humans
;
Intellectual Disability
;
Male
;
Phenotype
;
Repressor Proteins/genetics*
;
Sex Characteristics
;
Tooth Abnormalities
9.Identification of a novel variant of NHS gene underlying Nance-Horan syndrome.
Xiaowei CHEN ; Peiwen XU ; Jie LI ; Yuping NIU ; Ranran KANG ; Yuan GAO
Chinese Journal of Medical Genetics 2021;38(11):1077-1080
OBJECTIVE:
To explore the genetic basis for a pedigree affected with Nance-Horan syndrome.
METHODS:
Clinical manifestation of the patients was analyzed. Genomic DNA was extracted from peripheral blood samples of the pedigree members and 100 unrelated healthy controls. A panel of genes for congenital cataract was subjected to next-generation sequencing (NGS), and candidate variant was verified by Sanger sequencing and bioinformatic analysis based on guidelines of American College of Medical Genetics and Genomics (ACMG). mRNA expression was determined by reverse transcriptase-PCR (RT-PCR). Linkage analysis based on short tandem repeats was carried out to confirm the consanguinity.
RESULTS:
A small insertional variant c.766dupC (p.Leu256Profs*21) of the NHS gene was identified in the proband and his affected mother, but not among unaffected members and the 100 healthy controls. The variant was unreported in Human Gene Mutation Database (HGMD) and other databases. Based on the ACMG guideline, the variant is predicted to be pathogenic (PVS1+PM2+PM6+PP4).
CONCLUSION
The novel variant c.766dupC of the NHS gene probably underlay the X-linked dominant Nance-Horan syndrome in this pedigree.
Cataract/genetics*
;
Genetic Diseases, X-Linked
;
Humans
;
Mutation
;
Pedigree
;
State Medicine
;
Tooth Abnormalities
10.Prosthodontic treatment of congenital tooth agenesis I. The classicfication, prevalence and etiology of congenital tooth agenesis.
Chinese Journal of Stomatology 2011;46(1):54-57
Anodontia
;
classification
;
epidemiology
;
etiology
;
genetics
;
Genetic Diseases, X-Linked
;
etiology
;
genetics
;
Humans
;
Mutation
;
Prevalence
;
Tooth Abnormalities
;
etiology
;
genetics