Short stature and azoospermia in a patient with Y chromosome long arm deletion

被引:16
作者
De Rosa, M
De Brasi, D
Zarrilli, S
Paesano, L
Pivonello, R
D'Agostino, A
Longobardi, S
Merola, B
Lupoli, G
Ogata, T
Lombardi, G
机构
[1] Univ Naples Federico II, Dipartimento Endocrinol & Oncol Mol & Clin, Naples, Italy
[2] Univ Naples Federico II, Dipartimento Biol & Patol Mol & Cellulare, Naples, Italy
[3] Kejo Univ, Sch Med, Dept Paediat, Tokyo, Japan
关键词
short stature; Y chromosome; growth controlling gene; spermatogenesis; azoospermia;
D O I
10.1007/BF03346921
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
We report on a 42-year old male with short stature, azoospermia and a wide deletion of long arm of Y chromosome. On physical examination, the patient showed height of 149 cm (<1 degrees centile) and reduced volume (3 ml) and consistency of the testes. On hormonal evaluation, he showed increased serum gonadotropins and normal serum testosterone levels though its HCG stimulated levels were limited. Serum thyroid hormones were normal. Serum GH levels in baseline evaluation as well as after GHRH and GHRH + pyridostigmine administration were normal. Serum IGF I levels were lower than normal in baseline evaluation whereas its response to the GH administration was in the normal range. The bilateral testicular biopsy showed tubular atrophy, hyalinosis, interstitial sclerosis and a histological picture of a Sertoli cell only syndrome. Moreover the patient showed arthropathy, otopathy, small chin, small mouth and truncal obesity, On genetic evaluation, the patient showed a 46,X,delY(pter-->q11.1:) karyotype and loss of several DNA loci on Yq, In fact he preserved short arm SRY, centromeric DYZ3 and more proximal euchromatic region Yq loci, including DYS270, DYS271, DYS272, DYS11, DYS273, DYS274, DYS148, DYS275, and missed more distal DNA loci from DYS246 to DYZ2. These results disclosed a wide Y long arm deletion, including all hypothized Yq azoospermia loci (except for AZFa and probably for one of the RBM genes, which lie proximally to the deletion) and possibly the Y-specific growth control region (GCY), mapped between DYS11 and DYS246 loci. This deletion is responsible for the complete azoospermia of the patient and probably also for his short stature, even if other factors could be implicated in the statural impairment, It further possibly allowed to relate the GCY gene(s) to the control of GH or IGF-I receptor or post-receptor pathway, being the alteration of this gene(s) consistent with the hormonal pattern of the patient. (C) 1997, Editrice Kurtis.
引用
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页码:623 / 628
页数:6
相关论文
共 26 条
[1]  
Affara N, 1996, CYTOGENET CELL GENET, V73, P33
[2]  
ANDERSON M, 1988, HUM GENET, V79
[3]   Y-CHROMOSOME SPECIFIC PROBES IDENTIFY BREAKPOINT IN A 45,X/46,X,DEL (Y) (PTER-]Q11.1-) KARYOTYPE OF AN INFERTILE MALE [J].
BEVERSTOCK, GC ;
MACFARLANE, JD ;
VEENEMA, H ;
HOEKMAN, H ;
GOODFELLOW, PJ .
JOURNAL OF MEDICAL GENETICS, 1989, 26 (05) :330-342
[4]   A SYNOPSIS OF THE HUMAN Y-CHROMOSOME [J].
BUHLER, EM .
HUMAN GENETICS, 1980, 55 (02) :145-175
[5]   DELETED YQ IN THE STERILE SON OF A MAN WITH A SATELLITED Y-CHROMOSOME (YQS) [J].
CHANDLEY, AC ;
GOSDEN, JR ;
HARGREAVE, TB ;
SPOWART, G ;
SPEED, RM ;
MCBEATH, S .
JOURNAL OF MEDICAL GENETICS, 1989, 26 (03) :145-153
[6]   HUMAN MALE-FERTILITY - Y-LINKED GENES AND SPERMATOGENESIS [J].
CHANDLEY, AC ;
COOKE, HJ .
HUMAN MOLECULAR GENETICS, 1994, 3 :1449-1452
[7]   SHORT ARM DICENTRIC Y-CHROMOSOME WITH ASSOCIATED STATURAL DEFECTS IN A STERILE MAN [J].
CHANDLEY, AC ;
AMBROS, P ;
MCBEATH, S ;
HARGREAVE, TB ;
KILANOWSKI, F ;
SPOWART, G .
HUMAN GENETICS, 1986, 73 (04) :350-353
[8]   Y-chromosome deletions in idiopathic severe testiculopathies [J].
Foresta, C ;
Ferlin, A ;
Garolla, A ;
Rossato, M ;
Barbaux, S ;
DeBortoli, A .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 1997, 82 (04) :1075-1080
[9]   TOWARDS THE MOLECULAR LOCALIZATION OF THE AZF LOCUS - MAPPING OF MICRODELETIONS IN AZOOSPERMIC MEN WITHIN 14 SUBINTERVALS OF INTERVAL-6 OF THE HUMAN Y-CHROMOSOME [J].
MA, K ;
SHARKEY, A ;
KIRSCH, S ;
VOGT, P ;
KEIL, R ;
HARGREAVE, TB ;
MCBEATH, S ;
CHANDLEY, AC .
HUMAN MOLECULAR GENETICS, 1992, 1 (01) :29-33
[10]  
Menke DB, 1997, AM J HUM GENET, V60, P237