نتایج جستجو برای: polydactyly

تعداد نتایج: 1218  

Journal: :Journal of epidemiology and community health 1995
I Leck R J Lancashire

STUDY OBJECTIVES The aims were: (1) to compare the birth prevalence of malformations in different ethnic groups and (2) to explore the reasons for the ethnic variations found by examining birth prevalence in the offspring of matings between ethnic groups. DESIGN Analysis of data from a register of malformations and register of births. SETTING Birmingham, England. SUBJECTS A total of 432,7...

2012
Andrea Poretti Giuseppina Vitiello Raoul CM Hennekam Filippo Arrigoni Enrico Bertini Renato Borgatti Francesco Brancati Stefano D'Arrigo Francesca Faravelli Lucio Giordano Thierry AGM Huisman Miriam Iannicelli Gerhard Kluger Marten Kyllerman Magnus Landgren Melissa M Lees Lorenzo Pinelli Romina Romaniello Ianina Scheer Christoph E Schwarz Ronen Spiegel Daniel Tibussek Enza Maria Valente Eugen Boltshauser

Oral-Facial-Digital Syndrome type VI (OFD VI) represents a rare phenotypic subtype of Joubert syndrome and related disorders (JSRD). In the original report polydactyly, oral findings, intellectual disability, and absence of the cerebellar vermis at post-mortem characterized the syndrome. Subsequently, the molar tooth sign (MTS) has been found in patients with OFD VI, prompting the inclusion of ...

Journal: :The Journal of bone and joint surgery. British volume 1996
R P Agarwal D Jain C S Ramesh Babu R K Garg

A kindred of seven affected individuals in three generations is described with autosomal dominant inheritance of bilateral five-fingered hands, pedal polydactyly with syndactyly and agenesis of the tibia and of the lower end of the radius.

2013
Hajime Matsumine Masaki Takeuchi

BACKGROUND This study describes the use of a bioabsorbable suture for skin suturing during surgery for lateral ray polydactyly followed by favorable postoperative outcome without the need for postoperative suture removal. METHODS A 5-0 Vicryl Rapide suture was used for skin suturing during surgery for lateral ray polydactyly in 9 children (mean age, 12.4 mo). Children were allowed to walk and...

Journal: :Human molecular genetics 2005
Melissa A Fath Robert F Mullins Charles Searby Darryl Y Nishimura Jun Wei Kamal Rahmouni Roger E Davis Marwan K Tayeh Michael Andrews Baoli Yang Curt D Sigmund Edwin M Stone Val C Sheffield

McKusick-Kaufman syndrome (MKS) is an autosomal recessive disorder characterized by post-axial polydactyly, congenital heart defects and hydrometrocolpos, a congenital structural abnormality of female genitalia. Mutations in the MKKS gene have also been shown to cause some cases of Bardet-Biedl syndrome (BBS) which is characterized by obesity, pigmentary retinopathy, polydactyly, renal abnormal...

Journal: :Clinical genetics 2015
C Vanlerberghe L Faivre F Petit O Fruchart A-S Jourdain F Clavier S Gay S Manouvrier-Hanu F Escande

During limb development, the spatio-temporal expression of sonic hedgehog (SHH) is driven by the Zone of polarizing activity Regulatory Sequence (ZRS), located 1 megabase upstream from SHH. Gain-of-function mutations of this enhancer, which cause ectopic expression of SHH, are known to be responsible for congenital limb malformations with variable expressivity, ranging from preaxial polydactyly...

2016
Bin Wang Yutao Diao Qiji Liu Hongqiang An Ruiping Ma Guosheng Jiang Nannan Lai Ziwei Li Xiaoxiao Zhu Lin Zhao Qiang Guo Zhen Zhang Rong Sun Xia Li

Preaxial polydactyly (PPD) is inherited in an autosomal dominant fashion and characterized by the presence of one or more supernumerary digits on the thumb side. It had been identified that point mutation or genomic duplications of the long-range limb-specific cis-regulator - zone of polarizing activity regulatory sequence (ZRS) cause PPD or other limb deformities such as syndactyly type IV (SD...

2010
Hatice KOÇAK Gülay CEYLANER

The WAGR contiguous gene deletion syndrome is a combination of Wilms tumor, Aniridia, Genito-urinary abnormalities, and growth and mental Retardation which is invariably associated with an 11p13 deletion. This deletion included the PAX6 and WT1 genes as previously reported in typical WAGR patients. Ocular defects result from hemizygosity for the PAX6 gene. Urogenital and renal abnormalities and...

Journal: :Genetics 2001
R M Clark P C Marker E Roessler A Dutra J C Schimenti M Muenke D M Kingsley

The major locus for dominant preaxial polydactyly in humans has been mapped to 7q36. In mice the dominant Hemimelic extra toes (Hx) and Hammertoe (Hm) mutations map to a homologous chromosomal region and cause similar limb defects. The Lmbr1 gene is entirely within the small critical intervals recently defined for both the mouse and human mutations and is misexpressed at the exact time that the...

2016
Abir Lal Nath Shweta Nair Rajdeep Pal

A case of Peters anomaly with bilateral post axial polydactyly, convex soles, ocular hypertelorism, a low nasal bridge, retrognathia, undescended testis, microphthalmia and club foot was examined in a neonatal Indian baby girl who had been delivered in the hospital and admitted to the newborn unit. She died aged five days. There were no cases of Peters anomaly recorded in India according to a l...

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