OHSU has the only program in Oregon with full care for complex fetal conditions. This includes:

• Complications of twin pregnancies
• Congenital lung malformations
• Genitourinary conditions
• Heart conditions
• Infections
• Neurological disorders and brain differences
• Rare genetic conditions

Our team of specialists has the training and experience to care for and treat the conditions below and more.

A  |  B  |  C  |  F  |  G  |  H  |  I  |  L  |  N  |  O  |  P  |  R  |  S  |  T  |  V

A

• Absent cavum septum pellucidum (absent CSP)
• Agenesis of corpus callosum
• Alloimmunization
• Arthrogryposis

B

• Beckwith-Wiedemann syndrome
• Bowel atresias
• Bronchopulmonary sequestration (BPS)

C

• Chorioangioma
• Cleft lip, cleft palate and craniofacial disorders
• Clubfoot
• Coarctation of the aorta
• Complex single ventricle
• Congenital brain anomalies
• Congenital diaphragmatic hernia (CDH)
• Congenital high airway obstruction syndrome (CHAOS)
• Congenital hypothyroidism
• Congenital lung lesions
• Congenital pulmonary airway malformation (CPAM)
• Cystic fibrosis
• Cysts
• Cytomegalovirus

F

• Fetal anemia
• Fetal arrhythmia
• Fetal congenital thyroid disorder
• Fetal heart failure
• Fetal neck mass

G

• Gastroschisis

H

• Hemoglobinopathies
• Hemophilia
• Heterotaxy syndrome
• Hydrocephalus
• Hydronephrosis
• Hydrops
• Hypoplastic left heart syndrome (HLHS)
• Hypospadias

I

• Intestinal atresias

L

• Lower urinary tract obstruction (LUTO)

M

• Megacystis megacolon intestinal hypoperistalsis syndrome
• Metabolic disorders
• Micrognathia
• Microdeletion and microduplication syndromes, including 22q11.2 deletion syndrome
• Monosomy X (Turner syndrome)
• Mosaic chromosome conditions
• Muscular dystrophy
• Myelomeningocele
• Myotonic dystrophy
• Myotubular myopathy

N

• Neural tube defects
• Noonan syndrome

O

• Omphalocele
• Osteogenesis imperfecta

P

• Parvovirus
• Placenta abnormalities
• Pleural effusion
• Polycystic kidney disease

R

• Renal agenesis

S

• Sacrococcygeal teratoma
• Selective intrauterine growth restriction
• Septo-optic dysplasia (SOD)
• Sickle cell disease
• Skeletal dysplasias
• Smith-Lemli-Opitz syndrome
• Spina bifida
• Spinal muscular atrophy (SMA)

T

• Thalassemias
• Toxoplasmosis
• Tracheoesophageal fistula
• Transposition of the great arteries (TGA)
• Trisomy 13 (Patau syndrome)
• Trisomy 18 (Edwards syndrome)
• Trisomy 21 (Down syndrome)
• Tuberous sclerosis
• Tubulinopathies
• Tumors and other masses
• Twin-twin transfusion syndrome (TTTS)
• Twin reversed arterial perfusion (TRAP) sequence

V

• Vasa previa
• Ventriculomegaly