Polydactyly
PURPOSE: To compare outcomes of the Bilhaut procedure with outcomes of conventional resection and reconstruction in radial polydactyly types II and IV.[ncbi.nlm.nih.gov]
However, simple ray resection does not always give a natural postoperative appearance, especially for short-type polydactyly.[ncbi.nlm.nih.gov]
Among the postaxial polydactyly cases, type A was most prevalent at 69.8% and type B was witnessed in 30.2% of cases.[ncbi.nlm.nih.gov]
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Patau Syndrome
Patau syndrome has an incidence of 1/10.000-20.000, the clinical diagnosis being suggested by the triad cleft lip and palate, microphthalmia/anophthalmia and postaxial polydactyly[ncbi.nlm.nih.gov]
Cleft lip/palate, micro- or anophthalmia, coloboma (even in the absence of major brain malformations), regions of occipital cutaneous aplasia, postaxial polydactyly, cardiac[orpha.net]
It leads to a variety of abnormalities that include mental retardation, microcephaly, low-set ears, eye structural defects, polydactyly, and limb abnormalities The presence[icd9data.com]
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Pallister-Hall Syndrome
The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type- A/B; No phenotype prediction from the[ncbi.nlm.nih.gov]
GLI3 related disorders - Greig cephalopolysyndactyly syndrome ( GCPS ; MIM 175700), Pallister-Hall syndrome ( PHS : MIM 146510), polydactyly, postaxial, type A1 ( PAPA1 ;[ctgt.net]
Individuals with mild PHS may be incorrectly diagnosed as having isolated postaxial polydactyly type A.[ncbi.nlm.nih.gov]
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Meckel Syndrome
The pathologic reports revealed type I polycystic kidney, bile duct proliferation, fibrosis of the portal area, encephalocele and polydactyly.[ncbi.nlm.nih.gov]
. , , Source MeSH Abnormalities, Multiple Adult Dwarfism Encephalocele Female Humans Polycystic Kidney Diseases Polydactyly Syndrome Ultrasonography, Prenatal Pub Type(s)[unboundmedicine.com]
KEY WORDS: Meckel syndrome type 1 - Ultrasonography - Encephalocele - Polycystic kidney diseases - Polydactyly top of page[minervamedica.it]
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Central Polydactyly of Fingers
GLI3 related disorders - Greig cephalopolysyndactyly syndrome ( GCPS ; MIM 175700), Pallister-Hall syndrome ( PHS : MIM 146510), polydactyly, postaxial, type A1 ( PAPA1 ;[ctgt.net]
Living with What is polydactyly, and what types of polydactyly can be seen in Pallister-Hall syndrome? When someone has polydactyly, they have extra fingers and/or toes.[thinkgenetic.com]
Short rib-polydactyly syndrome (types I and II). Asphyxiating thoracic dystrophy. Otopalatodigital syndrome. Mesomelic dysplasia (Werner type). Trisomy 13.[fetalultrasound.com]
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Central Polydactyly of Toes
There are four types of preaxial polydactyly: Type I (PPD1): thumb/hallux polydactyly, type II (PPD2): polydactyly of triphalangeal thumb, type III (PPD3): polydactyly of[bmcpediatr.biomedcentral.com]
Living with What is polydactyly, and what types of polydactyly can be seen in Pallister-Hall syndrome? When someone has polydactyly, they have extra fingers and/or toes.[thinkgenetic.com]
Short rib-polydactyly syndrome (types I and II). Asphyxiating thoracic dystrophy. Otopalatodigital syndrome. Mesomelic dysplasia (Werner type). Trisomy 13.[fetalultrasound.com]
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Polydactyly of a Biphalangeal Thumb
Molecular analysis of non-syndromic preaxial polydactyly: preaxial polydactyly type-IV and preaxial polydactyly type-I.[ingentaconnect.com]
We report the familial occurrence of a unilateral thumb polydactyly type 4 of Wassel (12) or preaxial polydactyly type 1 of Temtamy (11).[ncbi.nlm.nih.gov]
type 1, bilateral Orphanet: ORPHA295146 GTR MeSH Orphanet C Clinical test, R Research test, O OMIM, G GeneReviews , V ClinVar C R O G V Polydactyly of a biphalangeal thumb[ncbi.nlm.nih.gov]
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Cystic Kidney Disease
ORPHA:3032 Synonym(s): Goldston syndrome Meckel syndrome type 7 Meckel-like syndrome type 1 Renal-hepatic-pancreatic dysplasia-Dandy-Walker cysts syndrome Prevalence: Inheritance[orpha.net]
KEY WORDS: Meckel syndrome type 1 - Ultrasonography - Encephalocele - Polycystic kidney diseases - Polydactyly top of page[minervamedica.it]
[…] dysplasia with or without prenatal oligohydramnios, central nervous system abnormalities (commonly Dandy-Walker malformation), congenital hepatic fibrosis, and absence of polydactyly[orpha.net]
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Acrocallosal Syndrome
The phenotypic spectrum of GLI3 morphopathies includes autosomal dominant preaxial polydactyly type-IV and postaxial polydactyly type A/B; no phenotypic prediction from the[doi.org]
DISCUSSION Reports to date document five missense mutations in the GLI3 gene, four in GCPS patients and one in a postaxial polydactyly type A/B patient. 3– 5 The mutation[doi.org]
There is insertional polydactyly with 2/3 and 3/4 syndactyly.[doi.org]
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Crossed Polysyndactyly
The resemblance of preaxial polydactyly type 4 and crossed polydactyly with Greig syndrome is discussed. These disorder may be allelic. Lippincott-Raven Publishers.[journals.lww.com]
[…] with postaxial polydactyly of the feet (Type II)[4].[jpgmonline.com]
Crossed polydactyly type I in a mother and son: an autosomal dominant trait? Am J Med Genet 1991;40:41–43. CrossRef PubMed Google Scholar 3.[link.springer.com]
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