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Clinodactyly

Known as: Finger clinodactyly 
An angulation of a digit at an interphalangeal joint in the plane of the palm (finger) or sole (toe). [pmid:16252026]
National Institutes of Health

Related topics

Related topics

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AMINOPTERIN SYNDROME SINE AMINOPTERINAarskog syndromeBlepharo-cheilo-dontic syndromeBrachydactyly, Type A1, B

Papers overview

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2011
2011
Down's syndrome associated with a balanced Robertsonian translocation 13;14 maternally transmitted in the product of a twin diamniotic pregnancy
RESUMEN Introduccion. Las traslocaciones robertsonianas balanceadas involucran al brazo largo de dos cromosomas acrocentricos; la… 
Review
2007
Review
2007
Hypomethylation in the 11p15 telomeric imprinting domain in a patient with Silver–Russell syndrome with a CSH1 deletion (17q24) renders a functional role of this alteration unlikely
Silver–Russell syndrome (SRS) is a clinical and genetic heterogeneous malformation syndrome. Patients show intrauterine and… 
2003
2003
Mosaicism del(8p)/inv dup(8p) in a dysmorphic female infant: a mosaic formed by a meiotic error at the 8p OR gene and an independent terminal deletion event
Various chromosomal rearrangements are associated with the distal 8p region. Among them are the inv dup(8p),1 del(8p22),2–5 and… 
1991
1991
Gene localization in a family with X-linked syndromal mental retardation (Prieto syndrome).
A mapping study was performed on a 3-generation Spanish family with X-linked syndromal mental retardation. Affected males have a… 
1987
1987
Interstitial deletion of chromosome 2 (p23p25).
We report a patient with a de novo interstitial deletion of the short arm of chromosome 2 (p23p25). The patient had microcephaly… 
1985
1985
Partial trisomy 12q24.31----qter.
Clinical details of a male child with the karyotype 46,XY,-4,+der(4),t(4;12) (p16;q24.31)mat are reported and compared with those… 
1981
1981
Keratosis palmaris et plantaris with clinodactyly. A distinct autosomal dominant genodermatosis.
Keratosis palmaris et plantaris and clinodactyly of the 5th finger was diagnosed in 11 members of a family with a typical pattern… 
1979
1979
The Summitt syndrome: observations on a third case.
A 6 1/2 year old male presented with acrocephaly, brachydactyly, clinodactyly, mild syndactyly of the hands and feet, genu valgum… 
1975
1975
Lethal faciocardiomelic dysplasia- a new autosomal recessive disorder.
Three male sibs from consanguienous parents were found to have a strikingly similar pattern of multiple congenital anomalies. The… 
1970
1970
Bilateral colobomas of iris and choroid. Association with partial deletion of a chromosome of group D.
A newborn child of healthy parents presented at birth with bilateral colobomas of iris and choroid associated with multiple…