Micropenis in a newborn with acrocallosal syndrome [3]

Genetic Counseling

Volumn 15, Issue 2, 2004, Pages 233-235

  Ikbal, M ^a   Tastekin, A ^a   Ors, Rahmi ^a,b  

^a ATATURK UNIVERSITY   (Turkey)

^b ATATÜRK UNIVERSITY   (Turkey)

Author keywords

[No Author keywords available]

Indexed keywords

FOLLITROPIN; LUTEINIZING HORMONE; TESTOSTERONE;

ACROCALLOSAL SYNDROME; AUTOSOMAL RECESSIVE DISORDER; CASE REPORT; CHROMOSOME ANALYSIS; CHROMOSOME HIGH RESOLUTION BANDING ANALYSIS; CLINICAL FEATURE; CORPUS CALLOSUM AGENESIS; CRANIOFACIAL MALFORMATION; EAR MALFORMATION; ECHOCARDIOGRAPHY; ECHOGRAPHY; FOLLITROPIN BLOOD LEVEL; FRONTAL BOSSING; GENITAL MALFORMATION; HOLOPROSENCEPHALY; HUMAN; HYPERTELORISM; INHERITANCE; KARYOTYPE; LETTER; LUTEINIZING HORMONE BLOOD LEVEL; MACROCEPHALY; MALE; MALFORMATION SYNDROME; MENTAL RETARDATION MALFORMATION SYNDROME; MICROPENIS; MOTOR RETARDATION; MUSCLE HYPOTONIA; NEWBORN; NIPPLE MALFORMATION; NUCLEAR MAGNETIC RESONANCE IMAGING; POLYDACTYLY; PSYCHOMOTOR RETARDATION; PTOSIS; SKELETON MALFORMATION; STRABISMUS; SYNDACTYLY; SYNDROME DELINEATION; TESTOSTERONE BLOOD LEVEL;

ABNORMALITIES, MULTIPLE; CORPUS CALLOSUM; HUMANS; INFANT, NEWBORN; MALE; MENTAL RETARDATION; PENIS; POLYDACTYLY; SYNDROME;

EID: 3142583474     PISSN: 10158146     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Letter

References (7)

1. COURTENS W., VAMOS E., CHRISTOPHE C., SCHINZEL A.: Acrocallosal syndrome in an Algerian boy born to consanguineous parents: review of the literature and further delineation of the syndrome. Am. J. Med. Genet., 1997, 69(1), 17-22.
2. DOSS B.J., JOLLY S., QURESHI F., JACQUES S.M., EVANS M.I., JOHNSON M.P., LAMPINEN J., KUPSKY W.J.: Neuropathologic findings in a case of OFDS type VI (Varadi syndrome). Am. J. Med. Genet., 1998, 77(1), 38-42.
3. MATHENY M., HALL B., MANALIGOD J.M.: Otolaryngologic aspects of oral-facial-digital syndrome. Int. J. Pediatr. Otorhinolaryngol., 2000, 53(1), 39-44.
4. NELSON M. M., THOMSON A.J.: The acrocallosal syndrome. Am. J. Med. Genet., 1982, 12, 195-199.
5. SCHINZEL A.: Postaxial polydactyly, hallux duplication, absence of the corpus callosum, macrencephaly and severe mental retardation: a new syndrome. Helv. Paediat. Acta., 1979, 34, 141-146.
6. TEMTAMY S.A., MEGUID N.A.: Hypogenitalism in the acrocallosal syndrome. Am. J. Med. Genet., 1989, 32(3), 301-305.
7. TUROLLA L., CLEMENTI M., TENCONI R.: How wide is the clinical spectrum of the acrocallosal syndrome? Report of a mild case. J. Med. Genet., 1990, 27(8), 516-518.