1287 SYNDROMES ASSOCIATED WITH POLYDACTYLY AND HYPOPITUITARISM
نویسندگان
چکیده
منابع مشابه
Hypopituitarism associated with myalgia.
A patient with panhypopituitarism who presented with muscle pain and stiffness is described. These symptoms responded rapidly to treatment with thyroxine and cortisone acetate. The association between muscle disease and hypopituitarism is briefly reviewed.
متن کاملComplex consanguinity associated with short rib-polydactyly syndrome III and congenital infection-like syndrome: a diagnostic problem in dysmorphic syndromes.
Short rib-polydactyly syndromes (SRPS) are a heterogeneous group of recessively inherited lethal skeletal dysplasias. Four types have been recognised. However, overlap in the clinical and radiological features of the four types has led to difficulties in distinguishing between them. The congenital infection-like syndrome is an autosomal recessive syndrome characterised by mental retardation, mi...
متن کاملMonomelic Ulnar Dimelia Associated with Ipsilateral Polydactyly: An Extraordinary Anomaly
Ulnar dimelia (mirror deformity) is a rare dysontogenetic deformity of the upper limb caused by an embryonic disturbance of the developing limb bud. It is characterized by two ulnae, the duplication of the ulnar halves of the carpus, metacarpals and phalanges, with the absence of the radius and thumb. It is commonly unilateral. This anomaly may be associated with shoulder dislocation, fibular d...
متن کاملHypopituitarism associated with cavernous sinus thrombosis. Report of a case.
Weisman (1944) described a boy with a cavernous sinus thrombosis, probably secondary to an empyema of the lung, who died 24 days after the start 0 of his illness and was found to have pituitary necrosis probably due to infarction. Bouche, Guiot, Carrez, Cotin, and Comoy (1964) gave an account of four patients, all of whom had long histories of headache, who developed the clinical signs of caver...
متن کاملEvaluation of an Infant with Cholestasis and Congenital Hypopituitarism
We are reporting an infant with persistent abnormal liver function, neonatal jaundice, and intermittent hypoglycemia. Evaluation confirmed congenital hypopituitarism, in the absence of congenital anomalies and midline defect. His jaundice and abnormal liver function improved after treatment with Levothyroxine and hydrocortisone.
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ژورنال
عنوان ژورنال: Pediatric Research
سال: 1985
ISSN: 0031-3998,1530-0447
DOI: 10.1203/00006450-198504000-01311