Biomaterial Database

[Apert's syndrome (acrocephalo-syndactyly). A case with 1 abnormal chromosome]. 1966

P Genest, and M A Mortezai, and M Tremblay

UI	MeSH Term	Description	Entries
D007223	Infant	A child between 1 and 23 months of age.	Infants
D007621	Karyotyping	Mapping of the KARYOTYPE of a cell.	Karyotype Analysis Methods,Analysis Method, Karyotype,Analysis Methods, Karyotype,Karyotype Analysis Method,Karyotypings,Method, Karyotype Analysis,Methods, Karyotype Analysis
D008297	Male		Males
D002869	Chromosome Aberrations	Abnormal number or structure of chromosomes. Chromosome aberrations may result in CHROMOSOME DISORDERS.	Autosome Abnormalities,Cytogenetic Aberrations,Abnormalities, Autosome,Abnormalities, Chromosomal,Abnormalities, Chromosome,Chromosomal Aberrations,Chromosome Abnormalities,Cytogenetic Abnormalities,Aberration, Chromosomal,Aberration, Chromosome,Aberration, Cytogenetic,Aberrations, Chromosomal,Aberrations, Chromosome,Aberrations, Cytogenetic,Abnormalities, Cytogenetic,Abnormality, Autosome,Abnormality, Chromosomal,Abnormality, Chromosome,Abnormality, Cytogenetic,Autosome Abnormality,Chromosomal Aberration,Chromosomal Abnormalities,Chromosomal Abnormality,Chromosome Aberration,Chromosome Abnormality,Cytogenetic Aberration,Cytogenetic Abnormality
D006801	Humans	Members of the species Homo sapiens.	Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000168	Acrocephalosyndactylia	Congenital craniostenosis with syndactyly.	Apert Syndrome,Pfeiffer Syndrome,Saethre-Chotzen Syndrome,Acrocephalosyndactyly (Apert),Acrocephalosyndactyly III,Acrocephalosyndactyly, Type 1,Acrocephalosyndactyly, Type 3,Acrocephalosyndactyly, Type I,Acrocephalosyndactyly, Type II,Acrocephalosyndactyly, Type III,Acrocephalosyndactyly, Type V,Acrocephaly, Skull Asymmetry, and Mild Syndactyly,Apert-Crouzon Disease,Chotzen Syndrome,Craniofacial-Skeletal-Dermatologic Dysplasia,Dysostosis Craniofacialis with Hypertelorism,Kurczynski Casperson Syndrome,Noack Syndrome,Syndactylic Oxycephaly,Acrocephalosyndactylias,Acrocephalosyndactylies, Type 1,Acrocephalosyndactylies, Type 3,Acrocephalosyndactylies, Type I,Acrocephalosyndactylies, Type II,Acrocephalosyndactylies, Type III,Acrocephalosyndactylies, Type V,Acrocephalosyndactyly IIIs,Apert Crouzon Disease,Disease, Apert-Crouzon,Noack Syndromes,Saethre Chotzen Syndrome,Syndactylic Oxycephalies,Syndrome, Apert,Syndrome, Chotzen,Syndrome, Kurczynski Casperson,Syndrome, Noack,Syndrome, Pfeiffer,Syndrome, Saethre-Chotzen,Syndromes, Noack,Type I Acrocephalosyndactylies,Type I Acrocephalosyndactyly,Type II Acrocephalosyndactylies,Type II Acrocephalosyndactyly,Type III Acrocephalosyndactyly,Type V Acrocephalosyndactylies,Type V Acrocephalosyndactyly
D025063	Chromosome Disorders	Clinical conditions caused by an abnormal chromosome constitution in which there is extra or missing chromosome material (either a whole chromosome or a chromosome segment). (from Thompson et al., Genetics in Medicine, 5th ed, p429)	Autosomal Chromosome Disorders,Chromosome Abnormality Disorders,Chromosomal Disorders,Autosomal Chromosome Disorder,Chromosomal Disorder,Chromosome Abnormality Disorder,Chromosome Disorder,Chromosome Disorder, Autosomal,Chromosome Disorders, Autosomal,Disorder, Chromosomal,Disorder, Chromosome,Disorder, Chromosome Abnormality,Disorders, Chromosomal,Disorders, Chromosome

Related Publications

P Genest, and M A Mortezai, and M Tremblay

["Apert's foot" (in acrocephalo-syndactyly) (author's transl)].

February 1978, Zeitschrift fur Orthopadie und ihre Grenzgebiete,

P Genest, and M A Mortezai, and M Tremblay

Acrocephalo-syndactyl (Apert's syndrome) - a case report.

August 1981, Indian journal of medical sciences,

P Genest, and M A Mortezai, and M Tremblay

[Acrocephalo-syndactyly. Apropos of a case with multiple synostoses].

March 1974, Pediatrie,

P Genest, and M A Mortezai, and M Tremblay

Brachycephaly and syndactyly: Apert's syndrome.

January 2008, Indian journal of dermatology, venereology and leprology,

P Genest, and M A Mortezai, and M Tremblay

[Acrocephalo-syndactylia or Apert's disease].

January 1951, Revista cubana de pediatria,

P Genest, and M A Mortezai, and M Tremblay

Demonstration of a case of acrocephalo syndactyly (maladie d'Apert).

March 1946, Gynaecologia. International monthly review of obstetrics and gynecology. Revue internationale mensuelle d'obstetrique et de gynecologie. Monatsschrift fur Geburtshilfe und Gynakologie,

P Genest, and M A Mortezai, and M Tremblay

[Observations on a case of acrocephalo-syndactyly with special reference to the oro-facial picture].

June 1968, Minerva stomatologica,

P Genest, and M A Mortezai, and M Tremblay

Tissue expansion for Apert's syndactyly.

June 1995, Journal of hand surgery (Edinburgh, Scotland),

P Genest, and M A Mortezai, and M Tremblay

[Acrocephalo-syndactyly and essential tremors in hereditary combination].

January 1960, Rivista di neurologia,

P Genest, and M A Mortezai, and M Tremblay

An unusual form of acrocephalo-syndactyly resembling the syndrome of Rubinstein and Taybi.

January 1968, Godisen zbornik na Medicinskiot fakultet vo Skopje,