Bilateral retinopathy, aplastic anaemia, and central nervous system abnormalities: a new syndrome?

نویسندگان

  • T Revesz
  • S Fletcher
  • L I al-Gazali
  • P DeBuse
چکیده

A male infant was found to have bilateral exudative retinopathy at 6 months of age. A month later severe aplastic anaemia was diagnosed, eventually leading to the infant's death. Additional features of this seemingly new syndrome were intrauterine growth retardation, fine sparse hair, fine reticulate skin pigmentation, ataxia because of cerebellar hypoplasia, cerebral calcifications, extensor hypertonia, and progressive psychomotor retardation.

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

منابع مشابه

Clinical and chromosome studies in Fanconi's aplastic anaemia.

A pernicious anaemia-like picture of the peripheral blood associated with congenital abnormalities was first described by Fanconi (1927) in three brothers. Since then a similar syndrome has been reported from many parts of the world under the title of Fanconi's aplastic anaemia. Gmyrek and Syllm-Rapoport (1964) have reviewed 152 cases in the literature in considerable detail. Bloom et al. (1966...

متن کامل

The Role of Central Nervous System and Hypothalamic-Pituitary-Gonadal (HPG) Axis Changes in the Occurrence of Polycystic Ovary Syndrome: A Narrative Review Article

Background and Objectives: Polycystic ovary syndrome (PCOS) is a common reproductive endocrine disorder, affecting at least 10% of women in reproductive age. It is associated with hyperandrogenism, obesity, menstrual iregularity and infertility. There are several hypotheses regarding the metabolic, genetic, epigenetic, and environmental causes of the disease. Although the main cause of the dise...

متن کامل

A case of sarcoma of the central nervous system presenting as a Guillain-Barré syndrome.

A case of widespread spinal sarcoma is described with meningeal infiltration, involvement of the anterior cranial fossa complicated by aplastic anaemia and visceral metastases.

متن کامل

Constitutional aplastic anaemia: a family with a new X linked variety of amegakaryocytic thrombocytopenia.

A family is described in which three male members died in early infancy with severe thrombocytopenia and a fourth in adolescence with aplastic anaemia. One child was investigated in detail and shown to have amegakaryocytic thrombocytopenia, progressing to pancytopenia as a result of bone marrow hypoplasia. His associated congenital abnormalities differed from those described in Fanconi's aplast...

متن کامل

Cytogenetic profile of aplastic anaemia in Indian children

BACKGROUND & OBJECTIVES Aplastic anaemia is a rare haematological disorder characterized by pancytopenia with a hypocellular bone marrow. It may be inherited/genetic or acquired. Acquired aplastic anaemia has been linked to many drugs, chemicals and viruses. Cytogenetic abnormalities have been reported infrequently with acquired aplastic anaemia. Majority of the studies are in adult patients fr...

متن کامل

ذخیره در منابع من


  با ذخیره ی این منبع در منابع من، دسترسی به آن را برای استفاده های بعدی آسان تر کنید

برای دانلود متن کامل این مقاله و بیش از 32 میلیون مقاله دیگر ابتدا ثبت نام کنید

ثبت نام

اگر عضو سایت هستید لطفا وارد حساب کاربری خود شوید

عنوان ژورنال:
  • Journal of medical genetics

دوره 29 9  شماره 

صفحات  -

تاریخ انتشار 1992