Congenital hypoplasia of the thumb is not a rare condition in clinical practice, but a familial occurrence of this condition is exceedingly rare.
We report a family with familial congenital hypoplasia of the thumb. In three generations, five members were proved to be affected and another two were presumed to be affected. To our surprise, a younger sister of the propositus had tetralogy of Fallot and triphalangeal thumbs on both hands.
References
1.
BENAZZI, RB, and E BERGQUIST (1970). Congenital Hypoplasia Along The Radial Ray. A Report of Two Cases, American Journal of Roentgenology Radium Therapy Nuclear Medicine, 110, 572-577.
2.
BILBREY, GL Capt (1966). Isolated Congenital Familial Thumb Deformities. Report of a Family, The New England Journal of Medicine, 274, 1057-1060.
3.
BLAUTH, W (1967). Der hypoplastische Daumen, Archive für Orthopädische und Unfall-Chirurgie, 62, 225-246.
4.
FERRIER, PE, L CRIPPA, S FERRIER, and M WYSS (1975). Aplasie des Pouces et Thrombocytopenic (FANCONI) Clinique Hematologique et Cytogenetique D’un Patient et de sa Famille. Journal de Genetique Humaine, 23, 103-106. (Suppl). (Fr).
5.
HOLMES, LB (1965). Congenital Heart Disease And Upper-Extremity Deformities. A Report of Two Families. The New England Journal of Medicine, 272, 437-444.
6.
HOLT, M, and S ORAM (1960). Familial Heart Disease With Skeletal Malformations. British Heart Journal, 22, 236-242.
7.
JOACHIMSTHAL, G (1895). Ueber angeborene Anomalien der oberen Extremitäten. Archiv fur Klinische Chirurgie, 50, 495-506.
8.
McKUSICK, VA (1961). Medical Genetics, 1960. Journal of Chronic Diseases, 14, 197-198101.
9.
SCHONENBERG, H (1968). Die Differentialdiagnose der Radialen Defektbildungen, Paediatrisch Praxis, 7, 455-467.
10.
STRAUCH, B, and M SPINNER (1976). Congenital Anomaly of the Thumb: Absent Intrinsics and Flexor Pollicis Longus. The Journal of Bone and Joint Surgery, 58-A, 115-118.
11.
UEJIMA, A, Y MIYAZAKI, and Y KOMATA (1978). A Family of Congenital Hypoplasia of the Thumb. Journal of Pediatrics, 31, 1901-1906. (Japanese).
12.
VEIT, G (1939). Uber familiares Vorkommen von Oligodaktylie, Z. Konstit. Lehr, 23, 630-635.
13.
ZETTERQVIST, P (1963). The Syndrome of Familial Atrial Septal Defect, Heart Arrhythmia and Hand Malformation (Holt-Oram) in Mother and Son. Acta Pediatrica, 52, 115-122.