Katzenstein M, Goodman R M
Newborn Nursery Unit, Meir Hospital, Sapir Medical Center, Kfar Sava, Israel.
J Craniofac Genet Dev Biol. 1988;8(2):111-26.
The Pena Shokeir type I syndrome is considered to be a lethal disorder in most cases. Infrequently, some of the affected children may reach the age of 1 year and beyond. When there is a history of another affected sib, the entity can be suspected prenatally. It is an uncommon autosomal recessive disorder. Out of 33 reported infants reviewed by us, six survived the neonatal period; among a further 27 cases, reported more recently, none survived the neonatal period. The clinical findings at birth are multiple and involve mainly the musculoskeletal and respiratory systems, accompanied by characteristic facial changes. The possibility of a primary hereditary malformation affecting the motor neuron cells of the spinal cord is postulated with the subsequent changes representing a fetal akinesia deformation sequence.
佩纳-绍凯尔I型综合征在大多数情况下被认为是一种致死性疾病。少数情况下,一些患病儿童可能活到1岁及以上。如果有其他患病同胞的病史,则可在产前怀疑该病。这是一种罕见的常染色体隐性疾病。在我们回顾的33例报告婴儿中,6例存活至新生儿期;在最近报告的另外27例病例中,无一例存活至新生儿期。出生时的临床表现多样,主要累及肌肉骨骼和呼吸系统,并伴有特征性面部改变。推测可能存在一种原发性遗传性畸形影响脊髓运动神经元细胞,随后的改变代表胎儿运动不能变形序列。