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Short 5th finger

Known as: Hypoplastic phalanges of the little finger, Fifth finger brachydactyly, Short pinky finger 
Hypoplasia (congenital reduction in size) of the fifth finger, also known as the little finger. [HPO:sdoelken]
National Institutes of Health

Related topics

Related topics

8 relations
Anonychia-onychodystrophy with hypoplasia or absence of distal phalangesChromosome 1p36 Deletion SyndromeHand foot uterus syndromeKabuki make-up syndrome

Papers overview

Semantic Scholar uses AI to extract papers important to this topic.
2018
2018
Eruptive syringomas in Down’s syndrome
Down’s syndrome is a common chromosomal anomaly associated with multiple malformations, medical conditions, and cognitive… 
2009
2009
Ring chromosome 21: A Case Report
Abstract In this article is reported, the phenotype of the male proband, with the ring configuration in chromosome 21. A 3½-year… 
2004
2004
A case report of a patient with retinoblastoma and chromosome 13q deletion: assignment of a new gene (gene for LCP1) on human chromosome 13
SummaryRetinoblastoma (Rb) occurs in hereditary, non-hereditary, and chromosomal deletion forms and the locus for the Rb gene (Rb… 
2003
2003
Corrections
Review
2000
Review
2000
Characterization of an interstitial deletion del(13)(q22q32) using microdissection and sequential FISH and G-banding.
The objective of this study was to delineate a chromosome 13 abnormality and establish its clinical correlation by using… 
1997
1997
Aarskog syndrome associated with hypermetropia and toe anomaly.
Aarskog syndrome is characterised by a disproportionately short stature and facial, skeletal and urogenital anomalies ('shawl… 
1987
1987
[The short little finger symptom in the Minkowski-Chauffard syndrome].
1987
1987
[The short little finger symptom in the Minkowski-Chauffard syndrome].
1984
1984
Congenital Heart Disease in a Case with Fetal Alcohol Syndrome: Clinical And Postmortem Findings
Clinical and autopsy findings of a male patient with fetal alcohol syndrome, centering on congenital heart disease, are reported. 
1980
1980
A case of multiple skeletal anomalies, ectodermal dysplasia, and severe growth and mental retardation.
A 17-year-old female patient presented extreme growth failure, severe microcephaly and developmental delay, and a unique pattern… 
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