Biomaterial Database

The Greig polysyndactyly-craniofacial dysmorphism syndrome. 1977

J P Fryns, and W Coeck, and H van den Berghe

A 15-month-old male child with the Greig polysyndactyly-craniofacial dysmorphism syndrome is presented and the relevant literature is reviewed.

UI	MeSH Term	Description	Entries
D007223	Infant	A child between 1 and 23 months of age.	Infants
D008297	Male		Males
D008607	Intellectual Disability	Subnormal intellectual functioning which originates during the developmental period. This has multiple potential etiologies, including genetic defects and perinatal insults. Intelligence quotient (IQ) scores are commonly used to determine whether an individual has an intellectual disability. IQ scores between 70 and 79 are in the borderline range. Scores below 67 are in the disabled range. (from Joynt, Clinical Neurology, 1992, Ch55, p28)	Disability, Intellectual,Idiocy,Mental Retardation,Retardation, Mental,Deficiency, Mental,Intellectual Development Disorder,Mental Deficiency,Mental Retardation, Psychosocial,Deficiencies, Mental,Development Disorder, Intellectual,Development Disorders, Intellectual,Disabilities, Intellectual,Disorder, Intellectual Development,Disorders, Intellectual Development,Intellectual Development Disorders,Intellectual Disabilities,Mental Deficiencies,Mental Retardations, Psychosocial,Psychosocial Mental Retardation,Psychosocial Mental Retardations,Retardation, Psychosocial Mental,Retardations, Psychosocial Mental
D005147	Facial Bones	The facial skeleton, consisting of bones situated between the cranial base and the mandibular region. While some consider the facial bones to comprise the hyoid (HYOID BONE), palatine (HARD PALATE), and zygomatic (ZYGOMA) bones, MANDIBLE, and MAXILLA, others include also the lacrimal and nasal bones, inferior nasal concha, and vomer but exclude the hyoid bone. (Jablonski, Dictionary of Dentistry, 1992, p113)	Bone, Facial,Bones, Facial,Facial Bone
D005385	Fingers	Four or five slender jointed digits in humans and primates, attached to each HAND.	Finger
D006801	Humans	Members of the species Homo sapiens.	Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000015	Abnormalities, Multiple	Congenital abnormalities that affect more than one organ or body structure.	Multiple Abnormalities
D012886	Skull	The SKELETON of the HEAD including the FACIAL BONES and the bones enclosing the BRAIN.	Calvaria,Cranium,Calvarium,Skulls
D013576	Syndactyly	A congenital anomaly of the hand or foot, marked by the webbing between adjacent fingers or toes. Syndactylies are classified as complete or incomplete by the degree of joining. Syndactylies can also be simple or complex. Simple syndactyly indicates joining of only skin or soft tissue; complex syndactyly marks joining of bony elements.	Polysyndactyly,Syndactylia,Syndactylias,Syndactylies
D013577	Syndrome	A characteristic symptom complex.	Symptom Cluster,Cluster, Symptom,Clusters, Symptom,Symptom Clusters,Syndromes

Related Publications

J P Fryns, and W Coeck, and H van den Berghe

The Greig polysyndactyly craniofacial dysmorphism syndrome: variable expression in a family.

May 1981, European journal of pediatrics,

J P Fryns, and W Coeck, and H van den Berghe

A newborn infant with craniofacial dysmorphism and polysyndactyly (Greig's syndrome).

March 1981, Acta paediatrica Scandinavica,

J P Fryns, and W Coeck, and H van den Berghe

A familial reciprocal translocation t(3;7) (p21.1;p13) associated with the Greig polysyndactyly-craniofacial anomalies syndrome.

November 1983, American journal of medical genetics,

J P Fryns, and W Coeck, and H van den Berghe

[Polysyndactyly-dysmorphic craniofacies, Greig type].

January 2001, Ryoikibetsu shokogun shirizu,

J P Fryns, and W Coeck, and H van den Berghe

Craniofacial dysmorphism in Apert syndrome.

January 2007, JBR-BTR : organe de la Societe royale belge de radiologie (SRBR) = orgaan van de Koninklijke Belgische Vereniging voor Radiologie (KBVR),

J P Fryns, and W Coeck, and H van den Berghe

[Greig's syndrome: variable polysyndactyly associated with distinct craniofacial dymorphism].

December 1982, Journal de genetique humaine,

J P Fryns, and W Coeck, and H van den Berghe

Novel GLI3 pathogenic variants in complex pre- and postaxial polysyndactyly and Greig cephalopolysyndactyly syndrome.

January 2021, American journal of medical genetics. Part A,

J P Fryns, and W Coeck, and H van den Berghe

Familial polysyndactyly and craniofacial anomalies.

January 1972, Clinical genetics,

J P Fryns, and W Coeck, and H van den Berghe

[Craniofacial dysmorphism with flexion of the fingers. Marden-Walker syndrome?].

November 1982, La semaine des hopitaux : organe fonde par l'Association d'enseignement medical des hopitaux de Paris,