نتایج جستجو برای: skeletal malformation

تعداد نتایج: 112139  

Journal: :The Saudi dental journal 2011
Ravi Prakash S Mohan Manu Dhillon Navneet Gill

The most common type of vascular malformation is the venous malformation and these are occasionally associated with phleboliths. We report a case of a 45 year old woman with intraoral venous malformation with phleboliths.

2016
Reid A. Maclellan Gulraiz Chaudry Arin K. Greene

UNLABELLED Primary lymphedema and capillary malformation are independent vascular malformations that can cause overgrowth of the lower extremity. We report a series of patients who had both types of malformations affecting the same leg. The condition is unique but may be confused with other types of vascular malformation overgrowth conditions (eg, Klippel-Trenaunay and Parkes Weber). METHODS ...

Journal: :American journal of medical genetics 1985
A Hunter

CARDIOVASCULAR DISORDERS cardiac congenital defects cardiopathy, congenital DERMATOLOGICAL DISORDERS cutis, dysplastic, not including ectodermal dysplasia cutis, aplasia, skin atrophy GENITAL DISORDERS genital dysfunctions hypogenitalism, hypogonadism; small testes, microorchidism, hypoplastic scrotum male genitalia, modifications not including ambiguity cryptorchidism JOINT DISORDERS joint, mo...

2013
Wei Shi Amanda L. Bain Bjoern Schwer Fares Al-Ejeh Corey Smith Lee Wong Hua Chai Mariska S. Miranda Uda Ho Makoto Kawaguchi Yutaka Miura John W. Finnie Meaghan Wall Jörg Heierhorst Carol Wicking Kevin J. Spring Frederick W. Alt Kum Kum Khanna

Single-stranded DNA binding proteins (SSBs) regulate multiple DNA transactions, including replication, transcription, and repair. We recently identified SSB1 as a novel protein critical for the initiation of ATM signaling and DNA double-strand break repair by homologous recombination. Here we report that germline Ssb1(-/-) embryos die at birth from respiratory failure due to severe rib cage mal...

2015
Katayoon Etemadi Behnaz Basir Safieh Ghahremani

BACKGROUND 49, XXXXY syndrome is a rare sex chromosomal disorder, occurring in 1 per 85,000-100,000 male births. The classical phenotype is ambiguous genitalia, facial dysmorphism, mental retardation and a combination of cardiac, skeletal and other malformations. CASE A two month-old boy with intrauterine growth restriction (IUGR) and low birth weight, facial dysmorphism, clinodactyly in feet...

Journal: :Jornal de pediatria 2003
Gilberto Pascolat José L Zindeluk Karen C Abrão Fabiana M Rodrigues Carolina I M Guedes

OBJECTIVE To report a case of rhizomelic chondrodysplasia punctata and present a brief literature review. DESCRIPTION The authors report the case of a 52-day-old child presenting the main findings of the syndrome: rhizomelic micromelia, characteristic facies, suction difficulty and anthropometric measures below the expected indexes for his age. Skeletal radiographies showed humeri and femora ...

Journal: :Revista espanola de cirugia ortopedica y traumatologia 2012
J M Gómez Fernández J M Méndez López F Caracuel Redondo

We report on a case of aplasia or unilateral congenital absence of the carpal scaphoid associated with dysplasia of the capitate. Congenital absence of the carpal scaphoid is a rare but well-documented condition. As far as we know, the present case is the seventh one reported in the medical literature. Imaging studies (X-ray and MRI) confirmed the absence of the carpal scaphoid associated with ...

2016
Erin L. Rutherford Laura Anne Lowery

Wolf-Hirschhorn Syndrome (WHS) is a neurodevelopmental disorder characterized by mental retardation, craniofacial malformation, and defects in skeletal and heart development. The syndrome is associated with irregularities on the short arm of chromosome 4, including deletions of varying sizes and microduplications. Many of these genotypic aberrations in humans have been correlated with the class...

Journal: :Dermato 2021

Klippel-Trenaunay syndrome (KTS) is a rare complex vascular with limb hypertrophy. KTS diagnosed if at least two of the three features capillary malformation, venous and soft tissue and/or bone overgrowth are present. Of these, malformation (i.e., port-wine stain) most commonly observed feature but may be absent in atypical KTS. We herein report case unilateral

Journal: :American journal of medical genetics 1985
G N Wilson A Raj D Baker

A new patient with trisomy for the chromosome segment 9pter----q22 is compared to 19 previously reported cases of partial trisomy 9. Manifestations such as microcephaly, prominent nasal root, bulbous nose, and down-turned corners of the mouth are common to patients with trisomic segments extending from 9p21 to 9q13, while intra-uterine growth retardation, cleft lip/palate, skeletal anomalies, a...

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