نتایج جستجو برای: rib polydactyly syndrome

تعداد نتایج: 631580  

Journal: :The Korean Journal of Pain 2016

Journal: :Clinical genetics 2013
C Thauvin-Robinet S Thomas M Sinico B Aral L Burglen N Gigot H Dollfus S Rossignol M Raynaud C Philippe C Badens R Touraine C Gomes B Franco E Lopez N Elkhartoufi L Faivre A Munnich N Boddaert L Van Maldergem F Encha-Razavi S Lyonnet M Vekemans E Escudier T Attié-Bitach

To the Editor : OFD1 mutations are responsible for X-linked dominant oral-facial-digital syndrome type I (OFDSI), as well as for four recessive X-linked phenotypes: mental retardation (MR) with macrocephaly, obesity, distal limb abnormalities and ciliary dysfunction [Simpson–Golabi–Behmel syndrome type 2 (SGBS2)], JS (Joubert syndrome) with polydactyly and retinal involvement (JBST10), an uncla...

Journal: :Indian pediatrics 2013
R Uppuluri K Gowrishankar L Janakiraman

Greig cephalopolysyndactyly syndrome is a rare genetic disorder, with an autosomal dominant inheritance and consisting of a triad of polysyndactyly, macrocephaly and hypertelorism. Crossed polydactyly is a finding characteristically associated with this syndrome. We report a one and half year old male child who presented with classic clinical features and family history diagnostic of the above ...

Journal: :Journal of medical genetics 1991
A Verloes S Aymé D Gambarelli M Gonzales M Le Merrer N Mulliez N Philip J Roume

A syndrome of holoprosencephaly and postaxial polydactyly, associated with hydrocephalus, heart defect, adrenal hypoplasia, and other visceral malformations, has been observed in five unrelated children with normal chromosomes. Clinical overlap with lethal acrodysgenital dwarfism (Smith-Lemli-Opitz syndrome type II) and hydrolethalus syndrome is discussed. Recessive inheritance seems likely.

2016
Sabitha Gokulraj N. Mohan J. Babususai Raj S. Yasmeen Ahamed C. J. Stephen Arokiaraj A. Cicilia Subbulakshmi

Ellis-Van Creveld syndrome or chondroectodermal dysplasia is a rare autosomal recessive disorder presenting several skeletal manifestations and congenital heart malformations. Ellis-Van Creveld syndrome comprises of a tetrad of clinical manifestations of chondrodysplasia, polydactyly, ectodermal dysplasia, and cardiac defects. Here, we are presenting a very rare case of Ellis-Van Creveld syndro...

Journal: :Journal of medical genetics 1999
A David P Bitoun D Lacombe J C Lambert A Nivelon J Vigneron A Verloes

McKusick-Kaufman syndrome (MKKS) is a rare, recessively inherited syndrome reported mainly in young children and is characterised by vaginal atresia with hydrometrocolpos, postaxial polydactyly, and congenital heart defect. Bardet-Biedl syndrome (BBS) is the generic name for a genetically heterogeneous group of autosomal recessive disorders characterised by retinal dystrophy or retinitis pigmen...

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