BIOMAT Database Logo BIOMAT Database Logo

[A case of congenital megakaryocytic thrombopenia associated with multiple malformations]. 1978

E Garibaldi, and G Chirico, and A Colombo

UI MeSH Term Description Entries
D007006 Hypogonadism Condition resulting from deficient gonadal functions, such as GAMETOGENESIS and the production of GONADAL STEROID HORMONES. It is characterized by delay in GROWTH, germ cell maturation, and development of secondary sex characteristics. Hypogonadism can be due to a deficiency of GONADOTROPINS (hypogonadotropic hypogonadism) or due to primary gonadal failure (hypergonadotropic hypogonadism). Hypergonadotropic Hypogonadism,Hypogonadism, Isolated Hypogonadotropic,Hypogonadotropic Hypogonadism,Hypogonadism, Hypergonadotropic,Hypogonadism, Hypogonadotropic
D007668 Kidney Body organ that filters blood for the secretion of URINE and that regulates ion concentrations. Kidneys
D008297 Male Males
D008533 Megakaryocytes Very large BONE MARROW CELLS which release mature BLOOD PLATELETS. Megakaryocyte
D001763 Blepharoptosis Drooping of the upper lid due to deficient development or paralysis of the levator palpebrae muscle. Ptosis, Eyelid,Blepharoptoses,Eyelid Ptoses,Eyelid Ptosis,Ptoses, Eyelid
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D003638 Deafness A general term for the complete loss of the ability to hear from both ears. Deafness Permanent,Hearing Loss Permanent,Prelingual Deafness,Deaf Mutism,Deaf-Mutism,Deafness, Acquired,Hearing Loss, Complete,Hearing Loss, Extreme,Acquired Deafness,Complete Hearing Loss,Deafness, Prelingual,Extreme Hearing Loss,Permanent, Deafness,Permanent, Hearing Loss,Permanents, Deafness
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

Related Publications

E Garibaldi, and G Chirico, and A Colombo
[Familial congenital thrombopenia associated with multiple osseous malformations].
January 1979, Revista de pediatrie, obstetrica si ginecologie. Pediatria,
E Garibaldi, and G Chirico, and A Colombo
[A case of congenital hypoplastic amegakaryocytic thrombopenia with skeletal and visceral malformations].
January 1968, Pediatrie,
E Garibaldi, and G Chirico, and A Colombo
[Syndrome of congenital thrombopenia with skeletal malformations].
April 1970, Pediatria polska,
E Garibaldi, and G Chirico, and A Colombo
[A case of multiple congenital malformations associated with partial acromegaloid manifestations].
September 1956, Rassegna di neurologia vegetativa,
E Garibaldi, and G Chirico, and A Colombo
[Case of multiple congenital malformations].
October 1950, La Presse medicale,
E Garibaldi, and G Chirico, and A Colombo
Female pseudohermaphroditism associated with multiple congenital malformations.
March 1972, Acta paediatrica Scandinavica,
E Garibaldi, and G Chirico, and A Colombo
Bilateral cryptophthalmos with multiple associated congenital malformations.
November 1985, Annals of plastic surgery,
E Garibaldi, and G Chirico, and A Colombo
Multiple congenital malformations associated with topical tretinoin.
April 1998, The Annals of pharmacotherapy,
E Garibaldi, and G Chirico, and A Colombo
[A rare case of multiple congenital malformations].
September 1966, Annali di stomatologia,
E Garibaldi, and G Chirico, and A Colombo
The multiple brain abscesses associated with congenital pulmonary arteriovenous malformations: a case report.
June 2002, Journal of Korean medical science,
Copied contents to your clipboard!