Asymmetry, Short Stature, and Variations in Sexual Development
- 1 May 1964
- journal article
- review article
- Published by American Medical Association (AMA) in American Journal of Diseases of Children
- Vol. 107 (5) , 495-515
- https://doi.org/10.1001/archpedi.1964.02080060497011
Abstract
In 1953, we described the first of a series of patients with congenital asymmetry, shortness of stature, and elevated urinary gonadotropins.65 Although the asymmetry in the original cases involved an entire side of the body, in some of the later ones 63,67,73 the variation in size was limited to the spine or the extremities. These reports also indicated that an increased excretion of gonadotropins represented only one of the variations in the pattern of sexual maturation that may occur in children with this Syndrome.* Other findings which were noted in many of the cases included small size at birth despite being born at term, the presence of café au lait areas of the skin, unusually short and/or incurved fifth fingers, a tendency for the face to be triangular with a broad forehead tapering down to a narrow chin, downturning of the corners of the mouth which has the shapeKeywords
This publication has 11 references indexed in Scilit:
- Low Birth Weight DwarfismArchives of Disease in Childhood, 1961
- PRECOCIOUS PUBERTY ASSOCIATED WITH HEPATOMAJournal of Clinical Endocrinology & Metabolism, 1959
- A CLINICAL ROUTINE-METHOD FOR THE QUANTITATIVE DETERMINATION OF GONADOTROPHINS IN 24-HOUR URINE SAMPLES, II: NORMAL VALUES FOR MEN AND WOMEN AT ALL AGE GROUPS FROM PRE-PUBERTY TO SENESCENCEActa Endocrinologica, 1959
- JUVENILE HYPOTHYROIDISM WITH PRECOCIOUS SEXUAL DEVELOPMENTJournal of Clinical Endocrinology & Metabolism, 1958
- CHROMOSOMAL SEX IN GONADAL DYSGENESIS (OVARIAN AGENESIS): RELATIONSHIP TO MALE PSEUDOHERMAPHRODISM AND THEORIES OF HUMAN SEX DIFFERENTIATION*†Journal of Clinical Endocrinology & Metabolism, 1955
- OVARIAN AGENESIS (CONGENITAL APLASTIC OVARIES) IN CHILDRENArchives of Pediatrics & Adolescent Medicine, 1953
- A NEW SYNDROME COMBINING DEVELOPMENTAL ANOMALIES OF THE EYELIDS, EYEBROWS AND NOSE ROOT WITH PIGMENTARY DEFECTS OF THE IRIS AND HEAD HAIR AND WITH CONGENITAL DEAFNESS - DYSTOPIA-CANTHI MEDIALIS ET PUNCTORUM LACRIMALIUM LATEROVERSA, HYPERPLASIA SUPERCILII MEDIALIS ET RADICIS NASI, HETEROCHROMIA IRIDUM TOTALIS SIVE PARTIALIS, ALBINISMUS CIRCUMSCRIPTUS (LEUCISMUS, POLIOSIS), ET SURDITAS CONGENITA (SURDIMUTITAS)1951
- NEUROFIBROMATOSIS (VON RECKLINGHAUSEN) AND OSTEITIS FIBROSA CYSTICA LOCALISATA ET DISSEMINATA (VON RECKLINGHAUSEN)Medicine, 1944
- THE EXCRETION OF GONADOTROPHIC HORMONE BY PREPUBERAL AND ADOLESCENT GIRLSJournal of Clinical Investigation, 1943
- A FURTHER STUDY OF THE NATURE OK HEMIIIYPERTROPHY WITH REPORT OF A NEW CASEThe Lancet Healthy Longevity, 1927