گزارش یک بیمار مبتلا به سندرم آلبرایت

Authors

  • حقیقتی, فریده
  • خورسند, افشین
Abstract:

Albright syndrome is a rare condition, usually appears in the early years of life and characterized by bending or thickening of long bones. In girls, of endocrine glands disorders especially precocious puberty are the most common symptoms. Also, Brown pigments in the skin are another sing of this syndrome. Certain mucosal and skin pigments are considerable features of the disease. Etiology and pathogenesis of this disease is not clear and various histopathologic patterns are observed. In fact, this disease is substitution of bone tissue with fibrous connective tissue in which various degrees of bone resorption and repair of the lesion is recognizable.

Upgrade to premium to download articles

Sign up to access the full text

Already have an account?login

similar resources

گزارش یک مورد سندرم آلبرایت

Mccune Albright syndrome is a polyosteotic fibrous dysplasia which manifests itself with disturbance of endocrine function and pigmented patch in skin at birth. The prevalence of polyosteotic is between two and three per million. The upper end of femur is the frequent site of involvement in polyosteotic form with multi endocrinopathy and limb deformity and multiple fractures. The presen...

full text

گزارش یک مورد سندرم آلبرایت

سندرم آلبرایت (mccune –albright) بیماری است که با فیبروز دیسپلازی منتشر، بلوغ جنسی زودرس و پیگمانتاسیون پوست تظاهر می کند. یافته های بالینی عبارتند از: پیگمانتاسیون پوست(café-au-lait) که در ابتدای تولد ظاهر می شود. 2- فیبروز دیسپلازی پلی استئوتیک که شایعتریـن محل درگیری آن پروگزیمال ران می باشــد 3- اختلال در کار غدد داخلی که به شکل پرکاری چند غده خود را نشان می دهد. 4- ناهنجاری اندامها و شکستگ...

full text

معرفی یک بیمار مبتلا به سندرم مافوچی

Introduction: Maffucci syndrome is a rare clinical entity (approximately 200 cases have been reported in the medical literature) with a combination occurrence of multiple enchodroma and vascular tumors. Case Report: Our patient was an 18 year old girl born in a non-consanguineous marriage with finger and toe bones disorders (enchondroma) causing deformity of fingers and toes with multiple vas...

full text

معرفی یک بیمار مبتلا به سندرم ایکتیوزلاملار

Introduction: Ichthyosis lamellar syndrome is a rare genodermatosis and in most families is inherited as an autosomal recessive trait because of transglutaminase-1 deficiency. Case Report: Our patient was a 6 year old girl and she was the result of consanguinity. She had large plate-like scales. The scales had mosaic-like pattern and erythroderma was absent. Tautness of her facial skin was as...

full text

مقایسه تأثیر وضعیت طاق باز و دمر بر وضعیت تنفسی نوزادان نارس مبتلا به سندرم دیسترس تنفسی حاد تحت درمان با پروتکل Insure

کچ ی هد پ ی ش مز ی هن ه و فد : ساسا د مردنس رد نامرد ي سفنت سرتس ي ظنت نادازون داح ي سکا لدابت م ي و نژ د ي سکا ي د هدوب نبرک تسا طسوت هک کبس اـه ي ناـمرد ي فلتخم ي هلمجزا لکتورپ INSURE ماجنا م ي دوش ا اذل . ي هعلاطم ن فدهاب اقم ي هس عضو ي ت اه ي ندب ي عضو رب رمد و زاب قاط ي سفنت ت ي هـب لاتـبم سراـن نادازون ردنس د م ي سفنت سرتس ي لکتورپ اب نامرد تحت داح INSURE ماجنا درگ ...

full text

My Resources

Save resource for easier access later

Save to my library Already added to my library

{@ msg_add @}


Journal title

volume 7  issue None

pages  47- 52

publication date 1994-06

By following a journal you will be notified via email when a new issue of this journal is published.

Keywords

No Keywords

Hosted on Doprax cloud platform doprax.com

copyright © 2015-2023