The Hoyeraal-Hreidarsson syndrome: The fourth case of a separate entity with prenatal growth retardation, progressive pancytopenia and cerebellar hypoplasia

Author:

Aalfs Cora M.,van den Berg Henk,Barth Peter G.,Hennekam Raoul C. M.

Publisher

Springer Science and Business Media LLC

Subject

Pediatrics, Perinatology, and Child Health

Reference12 articles.

1. Alter BP, Young NS (1993) The bone marrow failure syndromes. In: Nathan DG, Oshi FA (eds) Hematology of infancy and childhood. WB Saunders Company, Philadelphia, pp 216–316

2. Auerbach AD, Adler B, Chaganti RSK (1981) Prenatal and postnatal diagnosis and carrier detection of Fanconi anemia by a cytogenetic method. Pediatrics 67:128–135

3. Fanconi G (1927) Familiäre infantile perniciosaartige Anämie (perniziöses Blutbild und Konstitutin). Jahrb Kinderh 117:257–280

4. Giampietro PF, Adler-Brecher B, Verlander PC, Pavlakis SG, Davis JG, Auerbach AD (1993) The need for more accurate and timely diagnosis in Fanconi anemia: a report of the International Fanconi Anemia Registry. Pediatrics 91:1116–1120

5. Hoyeraal HM, Lamvik J, Moe PJ (1970) Congenital hypoplastic thrombocytopenia and cerebral malformations in two brothers. Acta Pediatr Scand 59:185–191

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