TY  - GEN
AU  - Ou-Yang,Mei-Chen
AU  - Yang,San-Nan
AU  - Hsu,Yung-Ming
AU  - Ou-Yang,Mei-Hui
AU  - Haung,Hsin-Chun
AU  - Lee,Shin-Yi
AU  - Hsieh,Wu-Shiun
AU  - Su,Yi-Ning
AU  - Liu,Chieh-An
TI  - Concomitant existence of total bowel aganglionosis and congenital central hypoventilation syndrome in a neonate with PHOX2B gene mutation
SN  - 1531-5037
PY  - 2007///0222
KW  - Disease Progression
KW  - Fatal Outcome
KW  - Hirschsprung Disease
KW  - complications
KW  - Homeodomain Proteins
KW  - genetics
KW  - Humans
KW  - Hypoventilation
KW  - Infant, Newborn
KW  - Male
KW  - Multiple Organ Failure
KW  - diagnosis
KW  - Mutation
KW  - Mutation, Missense
KW  - Rare Diseases
KW  - Risk Assessment
KW  - Syndrome
KW  - Transcription Factors
N1  - Publication Type: Case Reports; Journal Article
UR  - https://doi.org/10.1016/j.jpedsurg.2006.10.022
ER  -