Chaochun Zou
Biographic Data
| ID | 7612490 |
|---|---|
| NAME | Chaochun Zou |
| GIVEN NAMES | Chaochun |
| FAMILY NAME | Zou |
| SIGNATURE | ZOU C |
| AFFILIATIONS | Children's Hospital of Zhejiang University |
| ORCID | 0000-0002-4667-3636 |
| VERIFIED | Yes |
| TOTAL WORKS | 2 |
| TOTAL CITATIONS | 0 |
| WORKS AS AUTHOR | 2 |
| WORKS AS EDITOR | 0 |
| FIRST PUBLICATION YEAR | 2022 |
| LATEST PUBLICATION YEAR | 2023 |
| H-INDEX | 0 |
Health-related quality of life of children with Williams syndrome and caregivers in China
Introduction Williams syndrome (WS) is a rare genetic disorder that impacts multiple systems and may cause developmental delays. These medical and developmental issues impose a heavy burden on affected children and their families. However, there was no study on children’s health-related quality of life (HRQoL) with WS and only two studies about family quality of life globally. Therefore, the primary purpose of this study was to assess the HRQoL o…
Recombinant Human Growth Hormone Therapy for Childhood Trichorhinophalangeal Syndrome Type I
Trichorhinophalangeal syndrome type I (TRPS I; MIM 190350) is a rare autosomal dominant disorder of congenital malformations due to variants of the gene TRPS1. We reported on an 11-year-old Chinese boy with TRPS I. He had typical clinical findings, including sparse hair, a bulbous nose, a long philtrum, a thin upper lip, and skeletal abnormalities including cone-shaped epiphyses, shortening of the phalanges, and short stature. Trio whole exome se…
No prominent works on this page.
Recombinant Human Growth Hormone Therapy for Childhood Trichorhinophalangeal Syndrome Type I
Trichorhinophalangeal syndrome type I (TRPS I; MIM 190350) is a rare autosomal dominant disorder of congenital malformations due to variants of the gene TRPS1. We reported on an 11-year-old Chinese boy with TRPS I. He had typical clinical findings, including sparse hair, a bulbous nose, a long philtrum, a thin upper lip, and skeletal abnormalities including cone-shaped epiphyses, shortening of the phalanges, and short stature. Trio whole exome se…
Health-related quality of life of children with Williams syndrome and caregivers in China
Introduction Williams syndrome (WS) is a rare genetic disorder that impacts multiple systems and may cause developmental delays. These medical and developmental issues impose a heavy burden on affected children and their families. However, there was no study on children’s health-related quality of life (HRQoL) with WS and only two studies about family quality of life globally. Therefore, the primary purpose of this study was to assess the HRQoL o…
Medicine (2 works) · Bayesian multivariate linear regression (1 work) · Biology (1 work) · Bone age (1 work) · Brachydactyly (1 work) · Child Nutrition and Feeding Issues (1 work) · Clinical Psychology (1 work) · Endocrinology (1 work) · Exome sequencing (1 work) · Family and Disability Support Research (1 work)