Microcephaly with short stature, macrocytosis, and pancytopenia. 1993

M R DeBaun, and D A Wall, and M S Watson
Division of Hematology, St. Louis Children's Hospital, MO 63110.

UI MeSH Term Description Entries
D008297 Male Males
D008831 Microcephaly A congenital abnormality in which the CEREBRUM is underdeveloped, the fontanels close prematurely, and, as a result, the head is small. (Desk Reference for Neuroscience, 2nd ed.) Microlissencephaly,Severe Congenital Microcephaly,Congenital Microcephalies, Severe,Congenital Microcephaly, Severe,Microcephalies,Microcephalies, Severe Congenital,Microcephaly, Severe Congenital,Microlissencephalies,Severe Congenital Microcephalies
D010198 Pancytopenia Deficiency of all three cell elements of the blood, erythrocytes, leukocytes and platelets. Pancytopenias
D001827 Body Height The distance from the sole to the crown of the head with body standing on a flat surface and fully extended. Body Heights,Height, Body,Heights, Body
D002648 Child A person 6 to 12 years of age. An individual 2 to 5 years old is CHILD, PRESCHOOL. Children
D003937 Diagnosis, Differential Determination of which one of two or more diseases or conditions a patient is suffering from by systematically comparing and contrasting results of diagnostic measures. Diagnoses, Differential,Differential Diagnoses,Differential Diagnosis
D004913 Erythrocytes, Abnormal Oxygen-carrying RED BLOOD CELLS in mammalian blood that are abnormal in structure or function. Abnormal Erythrocytes,Abnormal Erythrocyte,Erythrocyte, Abnormal
D005199 Fanconi Anemia Congenital disorder affecting all bone marrow elements, resulting in ANEMIA; LEUKOPENIA; and THROMBOPENIA, and associated with cardiac, renal, and limb malformations as well as dermal pigmentary changes. Spontaneous CHROMOSOME BREAKAGE is a feature of this disease along with predisposition to LEUKEMIA. There are at least 7 complementation groups in Fanconi anemia: FANCA, FANCB, FANCC, FANCD1, FANCD2, FANCE, FANCF, FANCG, and FANCL. (from Online Mendelian Inheritance in Man, http://www.ncbi.nlm.nih.gov/entrez/dispomim.cgi?id Anemia, Fanconi,Fanconi Hypoplastic Anemia,Fanconi Pancytopenia,Fanconi Panmyelopathy,Fanconi's Anemia,Anemia, Fanconi's,Anemias, Fanconi,Fanconi Anemias
D006801 Humans Members of the species Homo sapiens. Homo sapiens,Man (Taxonomy),Human,Man, Modern,Modern Man

Related Publications

M R DeBaun, and D A Wall, and M S Watson
July 1981, Clinical genetics,
M R DeBaun, and D A Wall, and M S Watson
July 1994, Journal of child neurology,
M R DeBaun, and D A Wall, and M S Watson
February 1993, Anales de medicina interna (Madrid, Spain : 1984),
M R DeBaun, and D A Wall, and M S Watson
April 1997, Anales espanoles de pediatria,
M R DeBaun, and D A Wall, and M S Watson
December 2015, American journal of medical genetics. Part A,
M R DeBaun, and D A Wall, and M S Watson
January 1974, Birth defects original article series,
M R DeBaun, and D A Wall, and M S Watson
May 1992, Clinical genetics,
M R DeBaun, and D A Wall, and M S Watson
October 1975, Clinical genetics,
M R DeBaun, and D A Wall, and M S Watson
October 2016, European journal of medical genetics,
M R DeBaun, and D A Wall, and M S Watson
October 1997, Journal of medical genetics,
Copied contents to your clipboard!