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microcephaly
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microcephaly
microcephaly (maɪkrəʊˈsɛfəlɪ) Also in mod.L. form microcephalia. [ad. F. microcéphalie, f. mod.L. mīcrocephal-us: see microcephalous.] The condition of having an abnormally small head, esp. a. in Anthropology, having a skull of a capacity less than 1350 cubic centimetres (Flower Catal. Mus. Surg. 18...
Oxford English Dictionary
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Microcephaly
Mutations that result solely in microcephaly (primary microcephaly) exist but are less common. in mice, similar to human microcephaly.
wikipedia.org
en.wikipedia.org
Microcephaly in Children - Stanford Medicine Children's Health
Microcephaly is a condition where a baby's head is much smaller than normal. It is most often present at birth (congenital). Most children with microcephaly also have a small brain and intellectual disability. Some children with small heads have normal intelligence. Microcephaly may be caused by problems during a woman's pregnancy.
www.stanfordchildrens.org
Achalasia microcephaly
Achalasia microcephaly syndrome is a rare condition whereby achalasia in the oesophagus manifests alongside microcephaly and mental retardation. Microcephaly
Prenatal diagnosis of microcephaly is difficult due to the variability present in the causes of the disease.
wikipedia.org
en.wikipedia.org
Microcephaly albinism digital anomalies syndrome
Microcephaly albinism digital anomalies syndrome is a very rare congenital genetic disease. The syndrome includes microcephaly, micrognathia, oculocutaneous albinism, hypoplasia of the distal phalanx of fingers, and agenesia of the distal end
wikipedia.org
en.wikipedia.org
Microcephaly deafness syndrome
Microcephaly deafness syndrome is an extremely rare genetic disorder which consists of microcephaly, congenital hearing loss, mild intellectual disability References
Rare genetic syndromes
Syndromes with microcephaly
wikipedia.org
en.wikipedia.org
Microcephaly lymphoedema chorioretinal dysplasia
Microcephaly lymphoedema chorioretinal dysplasia also known as lymphedema microcephaly chorioretinopathy syndrome is a rare genetic condition associated A genetic association between microcephaly and lymphoedema.
wikipedia.org
en.wikipedia.org
Amish lethal microcephaly
Amish lethal microcephaly is a rare genetic disorder which is characterized by severe microcephaly (small head) from birth, brain hypoplasia (underdeveloped follows an autosomal recessive inheritance pattern
References
Autosomal recessive disorders
Rare genetic syndromes
Medical genetics
Syndromes with microcephaly
wikipedia.org
en.wikipedia.org
小头症 - World Health Organization (WHO)
小头症是新生儿小头或在出生后头部停止发育的一种疾病。. 小头症是一种罕见病。. 每几千名新生儿中,有一名新生儿患小头症。. 评估婴儿是否患小头症的最可靠方法是,在出生24小时后测量婴儿头围,将测量值与世卫组织生长标准对照,并在婴儿早期继续 ...
www.who.int
Aphalangy-syndactyly-microcephaly syndrome
aphalangia), syndactyly, duplication of the fourth metatarsal, microcephaly, and mild intellectual disabilities. References
Rare genetic syndromes
Autosomal dominant disorders
Syndromes with microcephaly
wikipedia.org
en.wikipedia.org
小头畸形的临床遗传学概述 - UpToDate
小头畸形是一种重要的神经系统表现。头部生长异常可能是潜在先天性、遗传性或获得性疾病的首个征象。很多遗传性疾病都与头部生长规律异常有关;越早发现这些疾病,就可越早提供恰当的治疗、服务和遗传咨询。本文将概述婴儿和儿童小头畸形的临床遗传学,其重点是对每个病例都尝试做出 ...
www.uptodate.com
Mandibulofacial dysostosis-microcephaly syndrome
Mandibulofacial dysostosis with microcephaly syndrome, also known as growth delay-intellectual disability-mandibulofacial dysostosis-microcephaly-cleft Signs and symptoms
People with this condition are usually born with congenital microcephaly, the type of microcephaly individuals with this condition
wikipedia.org
en.wikipedia.org
寨卡 (Zika) 病毒是怎么回事?
zika可以通过母婴传播进入已成型的婴儿体内,并影响婴儿的大脑发育,从而引发一种叫做Microcephaly症状,通俗地来说有这种症状的婴儿的头围(head circumference)变小(翻译经@julia chiu指正),更直接的说就是你的脑子会变小。 Microcephaly的成病因素有很多,与神经元的构成过程有关,与母亲的营养有关…总之并没有单一的原因而是有很多不同的因素互相影响孩子在子宫中的生长。
zhihu
www.zhihu.com
婴儿和儿童小头畸形的病因和评估 - UpToDate
婴儿和儿童小头畸形的病因和评估. 文献评审有效期至: 2023-11. 专题最后更新日期: 2022-07-15. 头围又称枕额头围 (occipitofrontal circumference, OFC),是直接反映头部生长的指标;测量头围是儿童生长发育评估的一个重要步骤。. 头部生长偏离正常轨迹可能是潜在先天性 ...
www.uptodate.com
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly
Infantile cerebral and cerebellar atrophy with postnatal progressive microcephaly is a rare hereditary autosomal recessive malformation syndrome of the References
Autosomal recessive disorders
Rare genetic syndromes
Syndromes with microcephaly
wikipedia.org
en.wikipedia.org