Radiographic characterization of the hands in Ritscher-Schinzel/3-C syndrome

نویسندگان

  • Kaitlyn J Friesen
  • Bernard N Chodirker
  • Albert E Chudley
  • Martin H Reed
  • Alison M Elliott
چکیده

ABSTRACT Ritscher-Schinzel Syndrome (RSS) is a clinically variable, autosomal recessive disorder, involving cardiac, cerebellar and craniofacial abnormalities. Numerous reports describe hand changes in RSS patients; however, a detailed characterization of the hands has not previously been performed. OBJECTIVE The purpose of this study was to identify whether specific radiographic hand changes were characteristic of RSS and could serve as a diagnostic tool. MATERIALS AND METHODS We performed a detailed radiographic hand characterization of 8 RSS patients. The patient population consisted of 5 males and 3 females from ages one month to 26 years, 7 months. The hands were characterized using metacarpophalangeal pattern (MCPP) profiles, carpal height and bone age analyses and assessment of bone morphology. RESULTS There was generalized brachydactyly with the second ray being the most severely affected. There was significant shortening of the first metacarpal and the fifth distal phalanx. The MCPP profile generated showed a consistent wavy pattern with average Z-scores ranging from -0.15 (4(th) proximal phalanx) to -2.13 (1(st) metacarpal) and 0.53 (4(th) middle phalanx) to -1.73 (2(nd) proximal phalanx) for the left and right hands, respectively. Six of eight patients showed a decreased carpal height. Bone age was within normal limits for all patients. Our study population showed consistent radiographic changes including: overtubulation of the bones (especially metacarpals 2-4), prominent tufts of the distal phalanges and a hypoplastic fifth distal phalanx. CONCLUSION The hand findings identified in this study can provide helpful diagnostic tools to clinicians when the diagnosis of RSS is being considered.

برای دانلود رایگان 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

On Hilbert Golab-Schinzel type functional equation

Let $X$ be a vector space over a field $K$ of real or complex numbers. We will prove the superstability of the following Go{l}c{a}b-Schinzel type equation$$f(x+g(x)y)=f(x)f(y), x,yin X,$$where $f,g:Xrightarrow K$ are unknown functions (satisfying some assumptions). Then we generalize the superstability result for this equation with values in the field of complex numbers to the case of an arbitr...

متن کامل

Cerebello-Cardiac) Syndrome: Case Report

Ritscher-Schinzel syndrome was first described 1987, in the case of two sisters of healthy parents who have had posterior fossa malformations, congenital heart defects and craniofacial anomalies (5). It is believed that this is an autosomal recessive hereditary disorder. So far, according to ORD data (Office of Rare Disease of the National Institutes of Health), only about 30 cases are reported...

متن کامل

The Role of Presence /Absence of Palmaris Longus and Fifth Flexor Digitorum Superfiscialis Tendons in Carpal Tunnel Syndrome

Background & Aims: Etiologically the causing factor of carpal tunnel syndrome is not clear and multiple contributing factors such as the presence or absence of Palmaris longus tendon have been cited. The aim of the present study was to compare patients with carpal tunnel syndrome and healthy individuals in regard to the absence and presence of Palmaris longus and fifth flexor digitarum superfic...

متن کامل

Scimitar Syndrome: Pathology, Clinical Presentation, Radiographic Features, and Treatment

Scimitar syndrome is characterized by partial or total anomalous pulmonary venous return from the right lung along with pulmonary hypoplasia.Wesearched the mail databases such as Medline (via PubMed), Scopus and EMBASE and Google Scholar. Diagnosing infantile scimitar syndrome requires meticulous attention and high suspicion of the early referral and management. The association of the syndrome ...

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

عنوان ژورنال:

دوره 2  شماره 

صفحات  -

تاریخ انتشار 2013