نقص صورت مرتبط با Abnomality مغزی Midline Facial Defects with Associated Brain Abnomality
- نوع فایل : کتاب
- زبان : انگلیسی
- ناشر : Elsevier
- چاپ و سال / کشور: 2018
توضیحات
رشته های مرتبط پزشکی
گرایش های مرتبط بیماری های اعصاب، پزشکی کودکان
مجله عصب شناسی کودکان – Pediatric Neurology
دانشگاه Chonbuk national university school of medicine – jeonju – Korea
منتشر شده در نشریه الزویر
کلمات کلیدی انگلیسی Chromosome 46, XX, del (18) (p11.1); Cleft lip; Holoprosencephaly; Malformation
گرایش های مرتبط بیماری های اعصاب، پزشکی کودکان
مجله عصب شناسی کودکان – Pediatric Neurology
دانشگاه Chonbuk national university school of medicine – jeonju – Korea
منتشر شده در نشریه الزویر
کلمات کلیدی انگلیسی Chromosome 46, XX, del (18) (p11.1); Cleft lip; Holoprosencephaly; Malformation
Description
A newborn girl weighing 2,700 g, born at 37 weeks 2 days of gestation to a 40-year-old multigravida mother via vaginal delivery was admitted to neonatal intensive care unit with cyanosis and morphologic anomalies. On physical examination, she showed hypotonia, microcephaly, low set ears, and midline facial defects such as single naris, depressed nasal ridge, and cleft lip (Figure 1). Brain MRI (magnetic resonance imaging) showed alobar holoprosencephaly with fused cerebral hemispheres and the thalamus shaped like a heart (Figure 2). Chromosomal analysis of her peripheral blood revealed 46, XX, del (18) (p11.1). Holoprosencephaly is a rare malformation of the human forebrain. This anomaly occurs due to failed cleavage of the prosencephalon early in gestation1,2 . Classically three subtypes have been recognized. The three main subtypes, in order of decreasing severity are alobar, semilobar, and lobar holoprosencephaly. It may be associated with other chromosomal anomalies such as trisomy 13, 18, chromosome 7q, 2q, or 18p deletion.
