Monosomy 5p

Monosomy 5p, also known as Cri du chat syndrome, is a rare autosomal deletion syndrome characterized by a mewing cry (cri du chat) in infancy, multiple congenital anomalies, intellectual disability, microcephaly, and facial dysmorphism.

Dysphagia

Difficulty in swallowing.


合計: 1

                       


（表示件数）
PMID (PMCID)
29853814
(5964566)
 MALE Infant, Newborn
Effects of Oral Stimulation Intervention in Newborn Babies with Cri du Chat Syndrome: Single-Subject Research Design.
Kim MK, Kim DJ.
Occup Ther Int. 2018;2018:6573508.
The purpose of this study is to treat dysphagia in a newborn baby with cri du chat syndrome using an oral stimulation intervention and to examine its effects.