Titlebook: Clinical Child Neurology; Mustafa A.M. Salih Book 2020 Springer Nature Switzerland AG 2020 DNA Technology.Evidence-based.Neurogenetic Diag

stress-response

Neurological Disorders in the Neonate, histories are also of paramount importance. For instance, previous neonatal deaths in the family may point towards metabolic autosomal recessive disorders, whilst details of any previous maternal miscarriages are especially relevant in suspected X-linked dominant disorders in which male lethality i

AMITY

Cranial Nerve Disorders,al sensation and movements, and swallowing. Localization is an important consideration in the management of these disorders, as well as the knowledge of the various diseases that cause cranial nerve dysfunction. There are 12 pairs of cranial nerves, which are numbered based on the order in which the

AVID

GNAT

Movement Disorders in Childhood, early development, unusual or paroxysmal movements during the preschool years, and the broad spectrum of movement patterns and mannerisms that typical children display. In differentiating benign from concerning movements, phenomenology (the appearance of the movement) is key. Although a good histor

輪流

Maximizer

Mystic

Developmental Delay and Intellectual Disability,tal domains: gross motor, fine motor, social and play, and speech and language. In addition, children progress in gaining skills in their cognitive abilities and behaviors throughout their lives which makes those two important aspects of children’s development and developmental assessment. It is ess

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Communication Disorders in Pediatrics, send, and process is impaired. Communication disorder may be evident in the process of speech, language, and/or hearing. Children acquire speech and language skills naturally without formal instruction; however, some children experience difficulties in their acquisition that vary in severity. It is

PALL

Autism Spectrum Disorder,with nonfunctional routines and abnormal stereotypic behaviors, with varying degree of impairment from people who need mild support to one who require a very substantial support. Although no definite cause is known yet, ASD is believed to have strong genetic bases, with concordance rate of 60–90% in

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