Congenital pyramidal signs and cerebellar ataxia with abnormal pyramidal decussation - A new syndrome

被引:0
|
作者
Castro Caldas, A.
Reimao, S.
Correia Guedes, L.
Miguel Rosa, M.
Ferreira, J.
Coelho, M.
机构
关键词
D O I
暂无
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
916
引用
收藏
页码:S356 / S356
页数:1
相关论文
共 50 条
  • [21] Abnormal Pyramidal Decussation and Bilateral Projection of the Corticospinal Tract Axons in Mice Lacking the Heparan Sulfate Endosulfatases, Sulf1 and Sulf2
    Aizawa, Satoshi
    Okada, Takuya
    Keino-Masu, Kazuko
    Doan, Tri Huu
    Koganezawa, Tadachika
    Akiyama, Masahiro
    Tamaoka, Akira
    Masu, Masayuki
    FRONTIERS IN MOLECULAR NEUROSCIENCE, 2020, 12
  • [22] Congenital fibrosis of the extraocular muscles (CFEOM) syndrome associated with progressive cerebellar ataxia
    Yoshida, Kunihiro
    Okano, Tomomi
    Hoshi, Kenichi
    Yahikozawa, Hiroyuki
    Suzuki, Kayo
    Banno, Haruhiko
    Tamura, Takuya
    Sobue, Gen
    Ikeda, Shu-ichi
    AMERICAN JOURNAL OF MEDICAL GENETICS PART A, 2007, 143A (13) : 1494 - 1501
  • [23] Pontine Malformation, Undecussated Pyramidal Tracts, and Regional Polymicrogyria: A New Syndrome
    Irahara, Kaori
    Saito, Yoshiaki
    Sugai, Kenji
    Nakagawa, Eiji
    Saito, Takashi
    Komaki, Hirofumi
    Nakata, Yasuhiro
    Sato, Noriko
    Baba, Kazumi
    Yamamoto, Toshiyuki
    Chan, Wai-Man
    Andrews, Caroline
    Engle, Elizabeth C.
    Sasaki, Masayuki
    PEDIATRIC NEUROLOGY, 2014, 50 (04) : 384 - 388
  • [24] CATARACT, DEAFNESS, CEREBELLAR ATAXIA, PSYCHOSIS AND DEMENTIA - A NEW SYNDROME
    STROMGREN, E
    DALBY, A
    DALBY, MA
    RANHEIM, B
    ACTA NEUROLOGICA SCANDINAVICA, 1970, 46 : 261 - +
  • [25] ABNORMAL PERISOMATIC STRUCTURES IN NON-PYRAMIDAL NEURONS IN THE CEREBRAL-CORTEX IN DOWNS-SYNDROME
    FABREGUES, I
    FERRER, I
    NEUROPATHOLOGY AND APPLIED NEUROBIOLOGY, 1983, 9 (02) : 165 - 169
  • [26] A novel de novo FEM1C variant is linked to neurodevelopmental disorder with absent speech, pyramidal signs and limb ataxia
    Dubey, Abhishek Anil
    Krygier, Magdalena
    Szulc, Natalia A.
    Rutkowska, Karolina
    Kosinska, Joanna
    Pollak, Agnieszka
    Rydzanicz, Malgorzata
    Kmiec, Tomasz
    Mazurkiewicz-Beldzinska, Maria
    Pokrzywa, Wojciech
    Ploski, Rafal
    HUMAN MOLECULAR GENETICS, 2023, 32 (07) : 1152 - 1161
  • [27] FAMILIAL AGENESIS OF CEREBELLAR VERMIS - A SYNDROME OF EPISODIC HYPERPNEA, ABNORMAL EYE MOVEMENTS, ATAXIA, AND RETARDATION
    JOUBERT, M
    EINSENRI.JJ
    ROBB, JP
    ANDERMAN.F
    NEUROLOGY, 1969, 19 (09) : 813 - &
  • [28] Prevalence of fragile X-associated tremor/ataxia syndrome: A survey of essential tremor patients with cerebellar signs or extrapyramidal signs
    Park, Ji-Hyung
    Jang, Wooyoung
    Youn, Jinyoung
    Ki, Chang-Seok
    Kim, Byoung Joon
    Kim, Hee-Tae
    Louis, Elan D.
    Cho, Jin Whan
    BRAIN AND BEHAVIOR, 2019, 9 (07):
  • [29] PPM-X: A new X-linked mental retardation syndrome with psychosis, pyramidal signs, and macroorchidism maps to Xq28
    Lindsay, S
    Splitt, M
    Edney, S
    Berney, TP
    Knight, SJL
    Davies, KE
    OBrien, O
    Gale, M
    Burn, J
    AMERICAN JOURNAL OF HUMAN GENETICS, 1996, 58 (06) : 1120 - 1126
  • [30] Autosomal dominant hydrocephalus with cerebral and cerebellar atrophyand ataxia: A new syndrome?
    Kwan, A
    Traynor, J
    Hudgins, L
    JOURNAL OF INVESTIGATIVE MEDICINE, 2004, 52 (01) : S132 - S132