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Biomedical subjects

A Ferrández

Publications and source records attributed to A Ferrández.

42 records · Page 3Linked to original sources

[Hypothyroidism acquired in childhood. Apropos of case].

Authors present a patient who, when three years old, was studied because of weight and psychic retardation. Physical data were as following: weight, 9.9 Kg (less than 93); height, 90 cm (P 10-25); head circumference, 43,5 cm (less than P3); bone age, 2 3/12 years, and the thyroid function, normal. I131 uptake, 43.5% after 24 h. TBI: T3 index, 1.07; T4, 7.7 gamma %. FT4 index, 7.2. Thyroid scan, normal. Diagnosis was: intrauterine dwarfism and iron-deficiency anemia. At 6 6/12 years old, he had measles and at this time his mother noted rapid weight gain, decrease in the grow rate, besides a coarse, cold skin and constipation, that did-not previously exist. Thyroid study showed typical primary hypothyroidism: I131 uptake, 14% after 24 h. TBI: T3 index, 1.2; T4, 1.2 micrograms/100. TSH in the test of TRH of 165 micro U/ml base and 245 maximum. Anti-thyroidal antibodies were negative. In view of the time coincidence, authors speculate that measles virus is perhaps the aetiologic agent of the hypothyroidism either directly or through an autoimmune reaction.

Body Weight↗

The trichorhinophalangeal syndrome. Report of 4 familial cases belonging to 4 generations.

Four familial cases of trichorhinophalangeal syndrome have been observed. These four and five other possible cases in the same family confirm the autosomal dominant inheritance and show a wide clinical expressivity. The radiological study of case 1 also confirms the existence of a characteristic generalized bone dysplasia. This syndrome bears in itself short stature of unknown etiology with normal growth hormone production. The skeletal deformities doe not affect the physical activity, and life span is not reduced.

Adult↗

Follow-up hormonal controls on a HGH secreting pituitary adenoma. Pre- and postoperative study.

The case of a 12 2/12-year-old boy with an HGH secreting eosinophilic adenoma is presented. The histologic investigation included conventional and ultrastructural techniques. The pre- and postoperative (1, 7, 11, and 20 months) hormonal controls are analyzed, indicating the persistence of HGH anteropituitary activity, even though surgical sectioning of the pituitary stalk was performed and the activities of thyroid, corticoadrenal and gonadotropin functions decreased. It is suggested that the hypothalamo-pituitary relationship may be maintained by extraportal venous circulations.

Adenoma↗

[Mitral echocardiography in hunter syndrome (author's transl)].

An echocardiographic study was realized in four patients with the Hunter syndrome (mucopolysaccharidoses II), evidenced by the clinical, radiologic and laboratory data. Mitral incompetence was present in two of the cases. In cases without mitral incompetence the echocardiographic tracing showed multiple mitral systolic echoes with a normal left atrium. On the other hand in cases with mitral incompetence the echocardiograms showed multiple systolic and diastolic echoes of the mitral valve with left atrial enlargement.

Child↗