Male siblings with dyserythropoiesis, microcephaly and intrauterine growth retardation

Clinical Dysmorphology

Volumn 11, Issue 2, 2002, Pages 107-111

  Okajima, K ^a   Ito, T ^a   Wakita, A ^a   Suzuki, Y ^a   Nagahama, M ^b   Shamoto, M ^c   Eguchi, M ^d   Wada, Y ^a  

^a NAGOYA CITY UNIV MEDICAL SCHOOL   (Japan)

^b INSTITUTE FOR DEVELOPMENTAL RESEARCH   (Japan)

^c FUJITA HEALTH UNIVERSITY   (Japan)

^d DOKKYO UNIVERSITY   (Japan)

Author keywords

Diarrhoea; Dyserythropoiesis; Liver dysfunction; Microcephaly

Indexed keywords

IRON;

ARTICLE; AUTOPSY; BONE MARROW EXAMINATION; CASE REPORT; CHROMOSOME ANALYSIS; CHRONIC DIARRHEA; COMPUTER ASSISTED TOMOGRAPHY; DYSERYTHROPOIESIS; FAILURE TO THRIVE; FETUS ECHOGRAPHY; HUMAN; HYDROPS; INTRAUTERINE GROWTH RETARDATION; IRON METABOLISM; LIVER DYSFUNCTION; MALE; MICROCEPHALY; MICROCYTOSIS; NEWBORN; NEWBORN JAUNDICE; NUCLEAR MAGNETIC RESONANCE IMAGING; OLIGOHYDRAMNIOS; OPTIC NERVE ATROPHY; PHOTOTHERAPY; PRIORITY JOURNAL; SECOND TRIMESTER PREGNANCY; SIBLING; BONE MARROW; BONE MARROW CELL; CONGENITAL DYSERYTHROPOIETIC ANEMIA; INFANT; PATHOLOGY; RADIOGRAPHY; ULTRASTRUCTURE;

ANEMIA, DYSERYTHROPOIETIC, CONGENITAL; AUTOPSY; BONE MARROW; BONE MARROW CELLS; FETAL GROWTH RETARDATION; HUMANS; INFANT; INFANT, NEWBORN; MALE; MICROCEPHALY;

EID: 0036009945     PISSN: 09628827     EISSN: None     Source Type: Journal    
DOI: 10.1097/00019605-200204000-00006     Document Type: Article

References (17)

1. Dyserythropoiesis associated with a Fas-deficient condition in childhood
2. Do some patients with Seckel syndrome have haematological problems and/or chromosome breakage?
3. A congenital dyserythropoietic anaemia variant presenting as hydrops foetalis
4. Type I congenital dyserythropoietic anaemia with myelopoietic abnormalities hand malformations
5. A patient with congenital dyserythropoietic anaemia type III presenting with stillbirths
6. Congenital dyserythropoietic anaemia (CDA) with intrauterine symptoms and early lethal outcome
7. Acral dysostosis dyserythropoiesis syndrome
8. Malignant lymphoma in congenital dyserythropoietic anaemia type III
9. An unusual variant of congenital dyserythropoietic anaemia with mild maternal and lethal fetal disease
10. Serum thymidine kinase in congenital dyserythropoietic anaemia type III
11. Intravascular haemolysis and increased prevalence of myeloma and monoclonal gammopathy in congenital dyserythropoietic anaemia, type III
12. A new type of congenital dyserythropoietic anaemia
13. Congenital dyserythropoietic anaemia type I presenting as persistent pulmonary hypertension of the newborn
14. Dyserythropoiesis and congenital dyserythropoietic anemias
15. Congenital dyserythropoiesis characterized by marked macrocytosis, vitamin B12- and folate-independent megaloblastic change and absence of the defining features of congenital dyserythropoietic anaemia types I or III
16. Composition of the intra-erythroblastic precipitates in thalassaemia congenital dyserythropoietic anaemia (CDA): Identification of a new type of CDA with intra-erythroblastic precipitates not reacting with monoclonal antibodies to -and -globin chains
17. Observations on two members of the Swedish family with congenital dyserythropoietic anaemia, type III