Biomaterial Database

[Bilateral anophthalmia in Fraser syndrome: report of a case]. 2013

Zouheir Hafidi, and Rajae Daoudi

Université Mohammed V Souissi, service d'ophtalmologie A de l'hôpital des spécialités, Centre hospitalier universitaire, Rabat, Maroc.

UI	MeSH Term	Description	Entries
D007231	Infant, Newborn	An infant during the first 28 days after birth.	Neonate,Newborns,Infants, Newborn,Neonates,Newborn,Newborn Infant,Newborn Infants
D003241	Consanguinity	The magnitude of INBREEDING in humans.	Inbreeding, Human,Consanguineous Marriage,Consanguinous Mating,Consanguineous Marriages,Consanguinities,Consanguinous Matings,Human Inbreeding,Human Inbreedings,Inbreedings, Human,Marriage, Consanguineous,Marriages, Consanguineous,Mating, Consanguinous,Matings, Consanguinous
D005260	Female		Females
D006801	Humans	Members of the species Homo sapiens.	Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man
D000853	Anophthalmos	Congenital absence of the eye or eyes.	Anophthalmia,Anophthalmias
D001003	Anal Canal	The terminal segment of the LARGE INTESTINE, beginning from the ampulla of the RECTUM and ending at the anus.	Anal Gland, Human,Anal Sphincter,Anus,Anal Gland,Anal Glands, Human,Detrusor External Sphincter,External Anal Sphincter,Internal Anal Sphincter,Anal Sphincter, External,Anal Sphincter, Internal,Anal Sphincters,Detrusor External Sphincters,External Anal Sphincters,Human Anal Gland,Human Anal Glands,Internal Anal Sphincters,Sphincter, Anal,Sphincter, Detrusor External,Sphincter, External Anal,Sphincter, Internal Anal,Sphincters, Anal
D014564	Urogenital Abnormalities	Congenital structural abnormalities of the UROGENITAL SYSTEM in either the male or the female.	Genitourinary Abnormalities,Abnormalities, Urogenital,Abnormalities, Genitourinary,Abnormality, Genitourinary,Abnormality, Urogenital,Genitourinary Abnormality,Urogenital Abnormality
D058497	Fraser Syndrome	Rare autosomal recessive congenital malformation syndrome characterized by cryptophthalmos, SYNDACTYLY and UROGENITAL ABNORMALITIES. Other anomalies of bone, ear, lung, and nose are common. Mutations on FRAS1 and FREM2 are associated with the syndrome.	Cryptophthalmos with Other Malformations,Cryptophthalmos-Syndactyly Syndrome,Cryptophthalmos Syndactyly Syndrome,Cryptophthalmos-Syndactyly Syndromes,Syndrome, Fraser