Zobrazeno 1 - 10
of 44
pro vyhledávání: '"Protuberant abdomen"'
Autor:
Montserrat Milà Recasens, Montserrat Izquierdo Renau, Josep Maria Martínez Crespo, Joan Sabrià Bach, Cristina Molinet Coll, Ana Alarcón Allen, Olga Gómez Del Rincón, David Monk
Publikováno v:
Journal of Clinical Ultrasound. 49:498-501
Kagami-Ogata syndrome (KOS14) is a rare congenital disorder associated with defective genomic imprinting of the chromosome 14q32 domain. Typical features include polyhydramnios, small and bell-shaped thorax, coat-hanger ribs, dysmorphic facial featur
Autor:
Munir Alam
Publikováno v:
International Journal of Innovative Research in Medical Science. 5
Objective / Purpose of the Study: For abdominal reshaping / contouring, patient with excess abdominal skin and redundant fat quite often require abdominoplasty / tummy tuck. Inconsistent results achieved with traditional liposuction especially in the
Publikováno v:
Journal of Fetal Medicine. :145-149
The purpose of this article is to analyse all cases of thanatophoric dysplasia and document the associated CNS anomalies. A retrospective study of all cases of thanatophoric dysplasia diagnosed in the department of perinatal pathology from January 20
Publikováno v:
Indian Journal of Child Health. :453-456
Thanatophoric dysplasia (TD) is a congenital, sporadic, and the most lethal skeletal dysplasia caused by new mutation in the fibroblast growth factor receptor 3 gene. At birth, it is characterized by shortening of the limbs (micromelia), small conica
Autor:
Pawan Kumar Vishwakarma, Ram Prakash Saha, Namita Chandra, Vaibhav Raj, Sanjay Kumar, Sheela Sinha
Publikováno v:
The American Journal of Case Reports
Patient: Female, 5 Final Diagnosis: Jarco-Levine syndrome Symptoms: Respiatory distress Medication: — Clinical Procedure: Supportive management Specialty: Pediatrics and Neonatology Objective: Congenital defects/diseases Background: Jarcho-Levin sy
Publikováno v:
Practical Diabetes. 34:132-134
Mauriac syndrome is an uncommon complication of poorly-controlled type 1 diabetes mellitus (T1DM) reported in children 13–17 years of age. It manifests as delayed growth, hepatomegaly, elevated liver enzymes and serum lipids, and glycogen accumulat
Autor:
Sherif A. Shazly, Diaa Eldeen M. Abd El Aal, Mahmoud A. Mahmoud Abd El Aleem, Ahmed M. Abbas, Mohammed K. Ali
Publikováno v:
Proceedings in Obstetrics and Gynecology. 5:1-6
Introduction: The presence of a thin-walled, multicystic structure posterior to the fetal head and neck with an intact vertebral column is known as a cystic hygroma. Thanatophoric dysplasia is the most lethal skeletal dysplasia. Thanatophoric dysplas
Publikováno v:
The New England journal of medicine. 378(4)
An Infant with Hypoglycemia A 5-month-old boy was admitted to the intensive care unit for evaluation of suspected hypoglycemia after several episodes of tachypnea in association with fasting. Examination revealed growth failure, doll-like facies, and
Publikováno v:
International Journal of Hematology. 93:253-256
A 62-year-old female suffering from rheumatoid arthritis(RA) for 16 years was referred to our hospital with out ofbreath on slight exertion. She had been prescribed withmethotrexate (MTX; 4 mg per week) and prednisolone for10 years for the treatment
Publikováno v:
Journal of Laboratory Physicians, Vol 6, Iss 02, Pp 121-123 (2014)
Journal of Laboratory Physicians
Journal of Laboratory Physicians
Thanatophoric dysplasia type 1 is a lethal congenital anomaly with skeletal dysplasia. It is characterized by short limb dwarfism, enlarged head with frontal bossing, short neck, protuberant abdomen. It is detected in early gestational period by ultr