Results 231 to 240 of about 3,414,711 (270)
Some of the next articles are maybe not open access.
Radiologic anthropometry of the hand in patients with familial short stature
Pediatric Radiology, 1988Fifth metacarpal bone shortening (brachymetacarpia V) was recently described to be highly prevalent in children with familial short stature (FSS). To characterize the hand bones of FSS patients with and without brachymetacarpia V, the left hand bone age radiographs of 26 FSS children were reviewed.
C D, Cervantes +2 more
openaire +2 more sources
Convergence of two types of familial short stature in a pedigree
Acta Endocrinologica, 1981Abstract. This study reports an unusual family with coexistence of isolated growth hormone deficiency transmitted as an autosomal dominant trait (Rimoin Type II) and constitutional short stature.
F, Mollica +4 more
openaire +2 more sources
A PSYCHOSOCIAL INTERVENTION PROGRAM FOR CHILDREN WITH SHORT STATURE AND THEIR FAMILIES
Social Work in Health Care, 1982A significant number of children with growth failure have primary or associated problems of a psychosocial nature. Ameliorating psychosocial complications is essential in assisting the child to reach an optimal level of development. This article describes a multidisciplinary program which provides a diagnostic evaluation to determine physical and ...
B S, Finley +2 more
openaire +2 more sources
Familial Trigonocephaly Associated With Short Stature and Developmental Delay
Archives of Pediatrics & Adolescent Medicine, 1981A family in which three male members had premature closure of the metopic suture with other suture involvement was studied. Each of the affected persons also had short stature and delayed development. The pattern of inheritance appeared to be X-linked recessive; however, the possibility of autosomal dominant inheritance with low expressivity in women ...
B, Say, J, Meyer
openaire +2 more sources
The Reassuring and Misleading Myth of Familial Short Stature
JAMA PediatricsN ...
Tamaro, Gianluca +2 more
openaire +3 more sources
Patients With Familial Short Stature: Correction and Clarification
Archives of Pediatrics & Adolescent Medicine, 1993Sir .—This is in response to the letter by Stanley M. Garn, PhD (written communication, March 24, 1992) regarding our article 1 published in the March 1992 issue of theArchives. The data throughout the article were indeed expressed as mean±SEM. However, a typographical mistake in the galley proof was not corrected; thus, the footnotes in Tables 1 and 3
openaire +2 more sources
Familial generalized delayed eruption of the dentition with short stature
Oral Surgery, Oral Medicine, Oral Pathology, 19761. Prolonged retention of the deciduous dentition, subsequent delay in eruption of the permanent dentition, and retardation in dental maturation are displayed outside the limits of normal variation. 2. The pedigree study of this family reveals the trait of noneruption to be distributed in a characteristic pattern of autosomal dominance. 3.
openaire +2 more sources
A Boy Presenting with Familial Short Stature - Diagnosis Gitelman Syndrome
Journal of Pediatric Endocrinology and Metabolism, 1999Patients with Gitelman syndrome are usually diagnosed by chance or present with muscular weakness, constipation, or tetanies due to hypokalemia and hypomagnesemia. We present a short statured boy with a clear history of familial short stature, normal growth and a final height prognosis within the target height range. However, routine laboratory studies
E, Schoof, M, Marx, H G, Doerr
openaire +2 more sources
Are Constitutional Delay of Growth and Familial Short Stature Different Conditions?
Clinical Pediatrics, 1980Children between 2 and 4 standard deviations below the mean height for age with no specific cause to account for their short stature are usually considered to represent either constitutional delay of growth (CDG) or familial short stat ure (FSS). This study was undertaken to determine whether 167 patients who were referred to our clinic for short ...
R, Lanes +4 more
openaire +2 more sources
A rare cause of syndromic short stature:
Abstract3M syndrome is a rare autosomal recessive genetic disorder characterized by severe growth retardation, dysmorphic facial features, skeletal dysplasia, and normal intelligence. Variants in CUL7, OBSL1, and CCDC8 genes have been reported to be responsible for this syndrome.
Esra Isik +9 more
openaire +4 more sources