Congenital dyserythropoietic anemia type I presenting as persistent pulmonary hypertension of the newborn

Hanna Shalev; Asher Moser; Joseph Kapelushnik; Michael Karplus; Nili Zucker; Isaac Yaniv; Hannah Tamary

doi:10.1016/S0022-3476(00)90025-8

Congenital dyserythropoietic anemia type I presenting as persistent pulmonary hypertension of the newborn

Hanna Shalev
, Asher Moser
, Joseph Kapelushnik
, Michael Karplus
, Nili Zucker
, Isaac Yaniv
, Hannah Tamary

Medical School for International Health

Research output: Contribution to journal › Article › peer-review

21 Scopus citations

Abstract

Congenital dyserythropoietic anemia (CDA) is a rare group of inherited bone marrow disorders characterized by anemia with ineffective erythropoiesis. We report 3 siblings from a family known to have CDA type I who presented with persistent pulmonary hypertension of the newborn (PPHN). We suggest that the diagnosis of CDA type I should be considered in any neonate with PPHN and anemia.

Original language	English
Pages (from-to)	553-555
Number of pages	3
Journal	Journal of Pediatrics
Volume	136
Issue number	4
DOIs	https://doi.org/10.1016/S0022-3476(00)90025-8
State	Published - 1 Jan 2000

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

SDG 3 Good Health and Well-being

ASJC Scopus subject areas

Pediatrics, Perinatology, and Child Health

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10.1016/S0022-3476(00)90025-8

Cite this

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title = "Congenital dyserythropoietic anemia type I presenting as persistent pulmonary hypertension of the newborn",

abstract = "Congenital dyserythropoietic anemia (CDA) is a rare group of inherited bone marrow disorders characterized by anemia with ineffective erythropoiesis. We report 3 siblings from a family known to have CDA type I who presented with persistent pulmonary hypertension of the newborn (PPHN). We suggest that the diagnosis of CDA type I should be considered in any neonate with PPHN and anemia.",

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T1 - Congenital dyserythropoietic anemia type I presenting as persistent pulmonary hypertension of the newborn

AU - Shalev, Hanna

AU - Moser, Asher

AU - Kapelushnik, Joseph

AU - Karplus, Michael

AU - Zucker, Nili

AU - Yaniv, Isaac

AU - Tamary, Hannah

PY - 2000/1/1

Y1 - 2000/1/1

N2 - Congenital dyserythropoietic anemia (CDA) is a rare group of inherited bone marrow disorders characterized by anemia with ineffective erythropoiesis. We report 3 siblings from a family known to have CDA type I who presented with persistent pulmonary hypertension of the newborn (PPHN). We suggest that the diagnosis of CDA type I should be considered in any neonate with PPHN and anemia.

AB - Congenital dyserythropoietic anemia (CDA) is a rare group of inherited bone marrow disorders characterized by anemia with ineffective erythropoiesis. We report 3 siblings from a family known to have CDA type I who presented with persistent pulmonary hypertension of the newborn (PPHN). We suggest that the diagnosis of CDA type I should be considered in any neonate with PPHN and anemia.

UR - https://www.scopus.com/pages/publications/0033926189

U2 - 10.1016/S0022-3476(00)90025-8

DO - 10.1016/S0022-3476(00)90025-8

M3 - Article

C2 - 10753260

AN - SCOPUS:0033926189

SN - 0022-3476

VL - 136

SP - 553

EP - 555

JO - Journal of Pediatrics

JF - Journal of Pediatrics

IS - 4

ER -

Congenital dyserythropoietic anemia type I presenting as persistent pulmonary hypertension of the newborn

Abstract

UN SDGs

ASJC Scopus subject areas

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