Abstract | PURPOSE: To describe the characteristics of type 0 ulnar longitudinal deficiency (ULD) in which deficiencies are present in the hand and carpus without involvement of the forearm or elbow. METHODS: A retrospective chart, radiograph, and clinical photograph review (1960-2005) of patients previously diagnosed with ectrodactyly, hand hypoplasia, or ULD was performed to evaluate for a diagnosis of ULD isolated to the hand. RESULTS: Thirteen extremities were identified. Three extremities had complete absence of the small-finger ray (phalanges and metacarpal) and 6 extremities had complete absence of the ring- and small-finger rays. Four hands showed hypoplasia of the small finger, 3 in conjunction with a ring- and small-metacarpal synostosis and 1 in isolation. Three extremities also had radial-sided hypoplasia or aplasia of the rays. Additional common findings included simple syndactyly, delta phalanx, and carpal fusions, most commonly of the capitohamate joint. CONCLUSIONS: Patients with isolated ulnar-sided hand deficiency such as ectrodactyly of the ring and/or small fingers or synostosis of the small metacarpal of the ring finger in the presence of a normal forearm may be diagnosed as having type 0 ULD. We propose that type 0 be added to the current classification systems for ULD representing those extremities with deficiencies isolated to the hand.
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Authors | Timothy G Havenhill, Paul R Manske, Archit Patel, Charles A Goldfarb |
Journal | The Journal of hand surgery
(J Hand Surg Am)
Vol. 30
Issue 6
Pg. 1288-93
(Nov 2005)
ISSN: 0363-5023 [Print] United States |
PMID | 16344190
(Publication Type: Journal Article)
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Topics |
- Female
- Hand Bones
(abnormalities)
- Hand Deformities, Congenital
(classification)
- Humans
- Male
- Retrospective Studies
- Syndactyly
(diagnosis)
- Synostosis
(diagnosis)
- Ulna
(abnormalities)
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