Table 1.

Pregnancy outcomes in inherited bone marrow failure syndromes

PatientDiagnosisFindings supportive of hematologic diagnosisMaternal age, yOutcomeNotes
TBD/DKC Telomere lengths well below first percentile in lymphocytes and granulocytes 29 IUFD at 20 WG Treated with epoetin alfa starting at 11 WG 
IUFD at 20 WG with fetal size consistent with GA of 17 wk 
32 SAB at 15 WG Bilateral fallopian tube recanalization/AMH: 1.4 ng/mL at 31 y of age 
Pregnancy through IVF 
SAB of 13-wk-sized fetus at 15 WG; growth lag noted at 12 WG 
TERC r.287C>G heterozygote 33 CS at 37 WG due to fetal intolerance of labor IUGR first percentile by 31 wk GA 
Transient, severe hypertension related to blood transfusion at 36 WG resulting in hospitalization for monitoring with induction of labor at 37 WG 
Low-birth-weight, female infant at 1970 g (less than first percentile) 
Insufficient milk to breastfeed 
TBD/DKC Telomere lengths well below first percentile in lymphocytes and granulocytes 17 Elective abortion At 23 y of age, found to have blocked fallopian tubes 
Early pulmonary fibrosis In her 30s, underwent IVF retrieval for fertility preservation prior to hematopoietic stem cell transplant; this was complicated by ascites related to liver cirrhosis; AMH: 0.5 ng/mL 
Liver cirrhosis 
Coats disease 
SDS Diagnosed in infancy with failure to thrive, exocrine pancreatic dysfunction, and malabsorption requiring prolonged G-tube placement 21 or 22 SAB at 6 WG NA 
Short adult height 23 CS at 39 WG due to fetal intolerance of labor 3080 g, male infant (29th percentile) 
Chorioamnionitis and funisitis 
Unable to breastfeed due to poor milk production 
28 SAB at 6 WG NA 
28 Repeat CS at 37 WG Fetus with hypoplastic left heart and growth restriction 
Mother treated for a breast infection and otitis externa after delivery 
DBA Blood transfusions as an infant (without anemia as an adult) 19 SVD at 39 WG 2582 g, female infant (sixth percentile) 
DBA Blood transfusions as a child 19 SAB at 8 WG NA 
35 SAB at 9 WG NA 
Family history of DBA 36 SAB at 11 WG NA 
36 Pregnant at study end NA 
DBA Managed with intermittent steroids and blood transfusions over years 17 Early SAB Spontaneous remission of DBA followed by relapse 
21 SAB at 12 WG Increased risk of Down syndrome on first trimester screen 
Normal fetal microarray with 2 regions of homozygosity >5 Mb noted 
DBA Managed with intermittent steroids and blood transfusions over years 22 Elective abortion Evaluated at 35 y of age for infertility; unable to conceive after this point 
SCN Neutropenia as an infant 28 CS at 41 WG for failure to progress in labor Treated with G-CSF throughout pregnancy 
Suffered recurrent infections until G-CSF available 3490 g, male infant (61st percentile) 
Son with SCN Mastitis requiring 2 admissions and leading to weaning within 3 months of delivery 
Poor wound healing at CS site 
PatientDiagnosisFindings supportive of hematologic diagnosisMaternal age, yOutcomeNotes
TBD/DKC Telomere lengths well below first percentile in lymphocytes and granulocytes 29 IUFD at 20 WG Treated with epoetin alfa starting at 11 WG 
IUFD at 20 WG with fetal size consistent with GA of 17 wk 
32 SAB at 15 WG Bilateral fallopian tube recanalization/AMH: 1.4 ng/mL at 31 y of age 
Pregnancy through IVF 
SAB of 13-wk-sized fetus at 15 WG; growth lag noted at 12 WG 
TERC r.287C>G heterozygote 33 CS at 37 WG due to fetal intolerance of labor IUGR first percentile by 31 wk GA 
Transient, severe hypertension related to blood transfusion at 36 WG resulting in hospitalization for monitoring with induction of labor at 37 WG 
Low-birth-weight, female infant at 1970 g (less than first percentile) 
Insufficient milk to breastfeed 
TBD/DKC Telomere lengths well below first percentile in lymphocytes and granulocytes 17 Elective abortion At 23 y of age, found to have blocked fallopian tubes 
Early pulmonary fibrosis In her 30s, underwent IVF retrieval for fertility preservation prior to hematopoietic stem cell transplant; this was complicated by ascites related to liver cirrhosis; AMH: 0.5 ng/mL 
Liver cirrhosis 
Coats disease 
SDS Diagnosed in infancy with failure to thrive, exocrine pancreatic dysfunction, and malabsorption requiring prolonged G-tube placement 21 or 22 SAB at 6 WG NA 
Short adult height 23 CS at 39 WG due to fetal intolerance of labor 3080 g, male infant (29th percentile) 
Chorioamnionitis and funisitis 
Unable to breastfeed due to poor milk production 
28 SAB at 6 WG NA 
28 Repeat CS at 37 WG Fetus with hypoplastic left heart and growth restriction 
Mother treated for a breast infection and otitis externa after delivery 
DBA Blood transfusions as an infant (without anemia as an adult) 19 SVD at 39 WG 2582 g, female infant (sixth percentile) 
DBA Blood transfusions as a child 19 SAB at 8 WG NA 
35 SAB at 9 WG NA 
Family history of DBA 36 SAB at 11 WG NA 
36 Pregnant at study end NA 
DBA Managed with intermittent steroids and blood transfusions over years 17 Early SAB Spontaneous remission of DBA followed by relapse 
21 SAB at 12 WG Increased risk of Down syndrome on first trimester screen 
Normal fetal microarray with 2 regions of homozygosity >5 Mb noted 
DBA Managed with intermittent steroids and blood transfusions over years 22 Elective abortion Evaluated at 35 y of age for infertility; unable to conceive after this point 
SCN Neutropenia as an infant 28 CS at 41 WG for failure to progress in labor Treated with G-CSF throughout pregnancy 
Suffered recurrent infections until G-CSF available 3490 g, male infant (61st percentile) 
Son with SCN Mastitis requiring 2 admissions and leading to weaning within 3 months of delivery 
Poor wound healing at CS site 

CS, cesarean section; DBA, Diamond-Blackfan anemia; GA, gestational age; G-tube, gastrostomy tube; IUFD, intrauterine fetal death; IUGR, intrauterine growth restriction; SAB, spontaneous abortion; SCN, severe congenital neutropenia; SDS, Shwachman-Diamond syndrome; SVD, spontaneous vaginal delivery; WG, weeks of gestation.

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