Metopic Craniosynostosis and Hydrocephalus in a Premature Opioid Dependent Baby
نویسندگان
چکیده
منابع مشابه
Microdeletion 9q22.3 syndrome includes metopic craniosynostosis, hydrocephalus, macrosomia, and developmental delay.
Basal cell nevus syndrome (BCNS), also known as Gorlin syndrome (OMIM #109400) is a well-described rare autosomal dominant condition due to haploinsufficiency of PTCH1. With the availability of comparative genomic hybridization arrays, increasing numbers of individuals with microdeletions involving this locus are being identified. We present 10 previously unreported individuals with 9q22.3 dele...
متن کاملpremature craniosynostosis in a rare genetic disease- a case report.
crouzon syndrome is a rare genetic disorder inherited in autosomal dominant pattern with complete penetration and variable expressivity. its most notable characteristic feature is premature synostosis of cranial sutures the case presented is of a 4 yr old boy with box like head with microcephaly, protuberant eyes, hydrocephalus, low visual acquity diagnosed as a case of crouzon syndrome after c...
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مقدمه: تولد یک نوزاد نارس تنش زیادی را برای والدین به همراه دارد. از جمله این موارد می توان نگرانی ازعوارض زایمان زودتر از موعد، احساس گناه مادر به دلیل احساس ناتوانی در به ثمر رساندن و تکمیل دوران بارداری، دور نمودن نوزاد از مادر بلافاصله پس از تولد برای مدت طولانی و مبهم بودن روند صحیح تکاملی را نام برد.
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Studies on children treated for craniosynostosis and hydrocephalus have focussed mainly on medical aspects in the past. However, in recent years the intellectual and social development of such children are also being studied. These children suffer from rejection since birth, due to obvious gross craniofacial deformity, brain anomalies and mental retardation(l). The intellectual deterioration is...
متن کاملPremature Craniosynostosis in a Rare Genetic Disease- A Case Report
BACKGROUND Crouzon syndrome is a rare genetic disorder inherited in autosomal dominant pattern with complete penetration and variable expressivity. Its most notable characteristic feature is premature synostosis of cranial sutures The case presented is of a 4 yr old boy with box like head with microcephaly, protuberant eyes, hydrocephalus, low visual acquity diagnosed as a case of crouzon syndr...
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ژورنال
عنوان ژورنال: Annals of Child Neurology
سال: 2020
ISSN: 2635-909X,2635-9103
DOI: 10.26815/acn.2020.00115