Biomaterial Database

[Changes in the facial skeleton in Apert-Crouzon's syndrome]. 1979

Iu M Aleksandrova, and N V Khoreva, and G M Petrunina

UI	MeSH Term	Description	Entries
D007574	Jaw Relation Record	A registration of any positional relationship of the mandible in reference to the maxillae. These records may be any of the many vertical, horizontal, or orientation relations. (Jablonski, Illustrated Dictionary of Dentistry)	Axiography,Bite Registration,Sirognathography,Record, Jaw Relation,Records, Jaw Relation,Bite Registrations,Jaw Relation Records,Registration, Bite,Registrations, Bite
D008297	Male		Males
D002508	Cephalometry	The measurement of the dimensions of the HEAD.	Craniometry
D002648	Child	A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL.	Children
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
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
D000293	Adolescent	A person 13 to 18 years of age.	Adolescence,Youth,Adolescents,Adolescents, Female,Adolescents, Male,Teenagers,Teens,Adolescent, Female,Adolescent, Male,Female Adolescent,Female Adolescents,Male Adolescent,Male Adolescents,Teen,Teenager,Youths
D012886	Skull	The SKELETON of the HEAD including the FACIAL BONES and the bones enclosing the BRAIN.	Calvaria,Cranium,Calvarium,Skulls
D014849	Waardenburg Syndrome	Rare, autosomal dominant disease with variable penetrance and several known clinical types. Characteristics may include depigmentation of the hair and skin, congenital deafness, heterochromia iridis, medial eyebrow hyperplasia, hypertrophy of the nasal root, and especially dystopia canthorum. The underlying cause may be defective development of the neural crest (neurocristopathy). Waardenburg's syndrome may be closely related to piebaldism. Klein-Waardenburg Syndrome refers to a disorder that also includes upper limb abnormalities.	Klein-Waardenburg Syndrome,Waardenburg's Syndrome,Klein Syndrome,Klein's Syndrome,Waardenburg Syndrome Type 1,Waardenburg Syndrome Type 3,Waardenburg Syndrome with Dystopia Canthorum,Waardenburg Syndrome with Upper Limb Anomalies,Waardenburg Syndrome, Type 1,Waardenburg Syndrome, Type 3,Waardenburg Syndrome, Type III,Waardenburg's Syndrome Type 1,Waardenburg-Klein Syndrome,White Forelock (Poliosis) Syndrome with Multiple Congenital Malformations,Klein Waardenburg Syndrome,Kleins Syndrome,Syndrome, Klein,Syndrome, Klein's,Syndrome, Klein-Waardenburg,Syndrome, Waardenburg,Syndrome, Waardenburg's,Syndrome, Waardenburg-Klein,Waardenburg Klein Syndrome,Waardenburgs Syndrome