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Internet resources relating to Syndactyly.
[OCOSH Code: D013576 373413006 Q70 HD_CHD_FD_SD]

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Acrocephalosyndactylia (7)
Craniostenosis characterized by acrocephaly and syndactyly, probably occurring as an autosomal dominant trait and usually as a new mutation.
Included Syndromes - Apert's, Pfeiffer Syndrome, Saethre-Chotzen Syndrome
MeSH Search Term "Acrocephalosyndactylia"[mesh]
ICD-10 Code Q87.0 Congenital malformation syndromes predominantly affecting facial appearance
SNOMED-CT Term Acrocephalosyndactyly (disorder) Concept ID: 268262006
Synonyms - Acrocephalosyndactyly
Apert's syndrome
Acrocephalosyndactyly (disorder)
OCOSH Code: D000168 268262006 Q87.0 HD_CHD_FD_SD_ACS
Poland Syndrome (2)
A syndrome which is characterized by symbrachydactyly and aplasia of the sternal head of pectoralis major.
MeSH Search Term "Poland Syndrome"[mesh]
ICD-10 Code Q79.8 Other congenital malformations of musculoskeletal system
SNOMED-CT Term Concept ID:
Synonyms -
OCOSH Code: D011045 373413006 Q79.8 HD_CHD_FD_SD
Syndactyly Patient Information (2)
Patient Information on the general topic of syndactyly OCOSH Code C05.116.099.370.894.819_bd_dbd_do_so_sd
OCOSH Code: C05.116.099.370.894.819_bd_dbd_do_so_sd

Resources

Birth- Syndactyly and delta phalanx

Location: http://www.e-hand.com/img/img00053.htm

The "delta bone" refers to a situation in which the middle bone in the finger is more of a triangular than a rectangular shape. This can occur with or without syndactyly. Although a delta bone results in a sideways curve of the finger, the joints on each end of the...
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View Details Visit Resource Review It Rate It Bookmark It Added: Thu Jan 31 2002

Cenani Syndactylism OMIM

Location: http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id=212780

Alternative titles; symbols
CENANI-LENZ SYNDACTYLY
SYNDACTYLY, TYPE VII
Cenani and Lenz (1967) described 2 brothers with a form of syndactyly resembling that of Apert syndrome (101200). However, additional features were severe shortening of the ulna and radius with fusion, fusion of the metacarpals and 'disorganization' of phalangeal development.
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Greig Cephalopolysyndactyly Syndrome

Location: http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Greig%20Cephalopolysyndactyly%20S ...

Craniofacial malformations, polysyndactyly. NORD Database.
Greig cephalopolysyndactyly syndrome (GCPS) is a rare genetic disorder characterized by physical abnormalities affecting the fingers and toes (digits) and the head and facial (craniofacial) area. Characteristic digital features may include extra (supernumerary) fingers and/or toes (polydactyly), webbing and/or fusion of the fingers and/or toes (syndactyly),...
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Greig cephalopolysyndactyly syndrome

Location: http://www.ojrd.com/content/3/1/10

The Greig cephalopolysyndactyly syndrome (GCPS) is a pleiotropic, multiple congenital anomaly syndrome. It is rare, but precise estimates of incidence are difficult to determine, as ascertainment is erratic (estimated range 1–9/1,000,000). The primary findings include hypertelorism, macrocephaly with frontal bossing, and polysyndactyly. The polydactyly is most commonly preaxial of the...
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Orocraniodigital Syndrome

Location: http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Orocraniodigital%20Syndrome

Cleft lip and palate, hypoplasia and/or syndactyly. Mental retardation. Orocraniodigital syndrome is an extremely rare inherited disorder characterized by multiple malformations of the head and face (craniofacial area) and the fingers and toes (digits). Major characteristics may include a vertical groove in the upper lip (cleft lip) and/or the inside,...
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Pallister-Hall Syndrome

Location: http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Pallister%20Hall%20Syndrome

Polysyndactyly, facial and brain abnormalities and imperforate anus. NORD Database
Pallister-Hall syndrome (PHS) is an extremely rare genetic disorder that may be apparent at birth (congenital). The symptoms and findings associated with the disorder may vary greatly in range and severity from case to case. However, in many individuals with Pallister-Hall...
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Pfeiffer Syndrome Orphanet

Location: http://www.pubmedcentral.nih.gov/articlerender.fcgi?artid=1482682

Pfeiffer syndrome is a rare autosomal dominantly inherited disorder that associates craniosynostosis, broad and deviated thumbs and big toes, and partial syndactyly on hands and feet. Hydrocephaly may be found occasionally, along with severe ocular proptosis, ankylosed elbows, abnormal viscera, and slow development. Based on the severity of the phenotype,...
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Saethre Chotzen Syndrome

Location: http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Saethre%20Chotzen%20Syndrome

craniosynostosis, causing the top of the head to appear pointed (acrocephaly), and/or webbing or fusion (syndactyly) of certain fingers or toes (digits). aka acrocephalosyndactyly type III. partial fusion of soft tissues (cutaneous syndactyly) of certain fingers and toes (digits); unusually short digits (brachydactyly); and broad great toes. NORD Database
Synonyms of...
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Summitt Syndrome

Location: http://www.rarediseases.org/search/rdbdetail_abstract.html?disname=Summitt%20Syndrome

Craniosynostosis and polysundactyly. May be one of the ACPS group of syndromes. NORD database.
Synonyms of Summitt Syndrome
* Summitt's Acrocephalosyndactyly
Summitt syndrome is an extremely rare genetic disorder characterized by malformations of the head, abnormalities of the hands and/or feet, and obesity. The syndrome is inherited as...
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Syndactyly eMedicine Orthopedics

Location: http://emedicine.medscape.com/article/1244420-overview

Syndactyly is the most common congenital malformation of the limbs, with an incidence of 1 in 2000-3000 live births. Syndactyly can be classified as simple when it involves soft tissues only and classified as complex when it involves the bone or nail of adjacent fingers. It is a shared feature...
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View Details Visit Resource Review It Rate It Bookmark It Added: Thu Apr 03 2008