Biomaterial Database

Melnick-Fraser syndrome. 2002

A Jayshree, and John Matthai

PSG Institute of Medical sciences and Research, Peelamedu, Coimbatore 641 004, Tamil Nadu. jayashwath@hotmail.com

UI	MeSH Term	Description	Entries
D002648	Child	A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL.	Children
D005260	Female		Females
D006801	Humans	Members of the species Homo sapiens.	Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D019280	Branchio-Oto-Renal Syndrome	An autosomal dominant disorder manifested by various combinations of preauricular pits, branchial fistulae or cysts, lacrimal duct stenosis, hearing loss, structural defects of the outer, middle, or inner ear, and renal dysplasia. Associated defects include asthenic habitus, long narrow facies, constricted palate, deep overbite, and myopia. Hearing loss may be due to Mondini type cochlear defect and stapes fixation. (Jablonski's Dictionary of Syndromes & Eponymic Diseases, 2d ed)	BOR Syndrome,Branchio-Oculo-Facial Syndrome,Branchio-Otorenal Dysplasia,BOF Syndrome,Branchial Clefts with Characteristic Facies, Growth Retardation, Imperforate Nasolacrimal Duct, and Premature Aging,Branchio-Otorenal Syndrome,Branchiooculofacial Syndrome,Branchiootorenal Dysplasia,Branchiootorenal Syndrome 1,Branchiootorenal Syndrome 2,Hemangiomatous Branchial Clefts-Lip Pseudocleft Syndrome,Lee Root Fenske Syndrome,Lip Pseudocleft-Hemangiomatous Branchial Cyst Syndrome,Melnick-Fraser Syndrome,Branchio Oculo Facial Syndrome,Branchio Oto Renal Syndrome,Dysplasia, Branchiootorenal,Hemangiomatous Branchial Clefts Lip Pseudocleft Syndrome,Lip Pseudocleft Hemangiomatous Branchial Cyst Syndrome,Melnick Fraser Syndrome,Syndrome, BOF