Baller-Gerold syndrome (BGS) is characterized by craniosynostosis and preaxial upper-limb malformations, and it has an autosomal recessive inheritance. Valproate syndrome occurs after exposure to valproic acid in utero, and is characterized by trigonocephaly. Both syndromes can also present with other malformations. Herein, we report a female newborn and her brother who both had a history of fe...

Nager syndrome is a rare syndrome resulting from developmental abnormalities of the first and second branchial arches. Nager syndrome is rare and mostly sporadic. The main clinical features consist of craniofacial, limb, and musculoskeletal morphogenesis. These findings included malar hypoplasia, maxillomandibular hypoplasia, micrognathia, downslanting palpebral fissures, cleft palate, ear anom...

Proc (Bayl Univ Med Cent) 2007;20:143–145 I n 1850 Dr. A. Notta, an “internè” in Paris, described four adult patients between the ages of 20 and 60 who had a nodule on a flexor tendon of a finger, thereby inhibiting its normal movement (1). This publication in the Archives Générales de Médecine led to these “nodules” being named “Notta’s nodules,” but a multitude of subsequent papers have large...

Pollicisation of the index finger for absence or severe hypoplasia of the thumb has been reported as a good procedure to recreate a new "thumb" with good cosmesis and acceptable function. The purpose of this study is to evaluate the outcome of our series. Seventeen patients with 24 involved hands agreed to come back for evaluation. The mean age at operation was 12 months. In 8 hands there was a...

The Yunis-Varón syndrome represents a rare autosomal recessive syndrome of easy recognition characterized by defective growth of the cranial bone along with complete or partial absence of the clavicles (cleidocranial dysplasia), absence of thumbs and halluces, distal aphalangia, ectodermal anomalies, growth retardation and poor outcome. The molecular genetic basis is unknown. Here, we report an...

conclusion our study revealed that the hypoplastic umbilical artery group’s non-dominant cia had higher ri values than the contralateral dominant cia. results eleven of the 165 patients (6.7%) demonstrated a hypoplastic umbilical artery. second-trimester us showed median dominant and non-dominant cia pi values of 1.43 and 1.60 (p = 0.062), respectively, and median dominant and non-dominant cia ...

  This case report presents a case of Fanconi’s Anemia with an unusual thumb polydactyly in a 2-year old boy. The extra thumb had no nail, nail bed and distal phalanx. The extra thumb had no active motion.The duplication of the thumb occurred at the carpometacarpal joint but its morphology did not match with any classification described for thumb polydactyly. Although his thumb polydactyly was ...

PURPOSE To evaluate clinical and cosmetic outcomes of reconstruction in thumb polydactyly and prognostic value of the Wassel classification. METHODS Between 1993 and 2000 inclusive, out of the patients with thumb polydactyly (involving 80 thumbs) operated on, 34 patients (36 thumbs) were available for review and underwent clinical and radiological assessment. Outcomes in terms of the Tada sco...

radial polydactyly, the most common digital duplication in asian and white populations, has a wide range of manifestations. its classification is useful for planning and assessing surgical treatment. our patient had four thumbs, duplicated radial carpal bones, and a bifurcated radius. this presentation is not covered by any of the current classifications. to the best of our knowledge, this is t...