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Clinodactyly of the 5th finger

Known as: Clinodactyly of fifth fingers, Bilateral clinodactyly of the fifth fingers, Bilateral fifth digit clinodactyly 
Clinodactyly refers to a bending or curvature of the fifth finger in the radial direction (i.e., towards the 4th finger). [HPO:curators, pmid… 
National Institutes of Health

Related topics

Related topics

50 relations
Acrocallosal SyndromeBloom SyndromeCatel Manzke syndromeCerebrocostomandibular Syndrome

Papers overview

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2013
2013
Caracterización molecular por aCGH de alteraciones genómicas en pacientes con discapacidad intelectual y malformaciones múltiples de etiología desconocida.
Proposito y Metodo del Estudio: Las alteraciones genomicas son la principal causa de anomalias congenitas y del desarrollo como… 
2011
2011
Craniofacial Morphology and Dental Findings of Seckel Syndrome: Case Reports of Two Siblings
Seckel Syndrome (SS) is a rare form of primordial autosomal recessive dwarfism involving multiple malformations. The major… 
2011
2011
指間形成術後の創部瘢痕拘縮による clinodactyly を認めた症例に逆行性指動脈島状皮弁を行った1例
2004
2004
Case reports Single maxillary central incisor in a girl with del( l8p) syndrome
We present a girl with del(18p) syndrome and a single maxillary central incisor; she is only the second patient in whom this… 
2002
2002
Bowen-Conradi syndrome.
The Bowen-Conradi syndrome is a severe genetic condition characterized by intrauterine growth retardation, failure to thrive… 
2002
2002
Investigation of the GRB 2 , GRB 7 , and CSH 1 genes as candidates for the Silver-Russell syndrome ( SRS ) on chromosome 17 q
Silver-Russell syndrome (SRS) (MIM 180860) is characterised by intrauterine and postnatal growth restriction, in association with… 
2000
2000
Atypical clinical picture of the Nijmegen breakage syndrome associated with developmental abnormalities of the brain
EDITOR—Nijmegen breakage syndrome (NBS) (OMIM 251260) is a rare autosomal recessive condition. The major manifestations include… 
1989
1989
Acrocallosal syndrome in a girl born to consanguineous parents.
The present report describes on a 1-year-old girl with macrocephaly, bulging forehead, ocular hypertelorism, antimongoloid… 
1985
1985
An autosomal dominant syndrome of characteristic facial appearance, preauricular pits, fifth finger clinodactyly, and tetralogy of Fallot.
This report describes six relatives with a syndrome of mild prenatal-onset growth deficiency, an altered craniofacial appearance… 
1975
1975
Trisomy iop. A report of two cases due to a familial translocation rcp (10;21) (pII;pII).
Trisomy for the short arm of chromosome number 10 was diagnosed (by a G-banding method) in two sisters with multiple congenital…