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"Laurin-Sandrow Syndrome - a review of the literature and classification system".
Buzea C, Boulanger N. Buzea C, et al. Clin Dysmorphol. 2022 Jul 1;31(3):109-112. doi: 10.1097/MCD.0000000000000420. Epub 2022 Mar 7. Clin Dysmorphol. 2022. PMID: 35256564 Review.
INTRODUCTION: Laurin-Sandrow syndrome also known as tetramelic mirror-image polydactyly is a rare congenital disorder characterized classically by polysyndactyly of the hands, mirror feet and nose anomalies (hypoplasia of the nasal alae and short columella) often associated with …
INTRODUCTION: Laurin-Sandrow syndrome also known as tetramelic mirror-image polydactyly is a rare congenital disorder characterized classica …
Fibular a/hypoplasia: review and documentation of the fibular developmental field.
Lewin SO, Opitz JM. Lewin SO, et al. Am J Med Genet Suppl. 1986;2:215-38. doi: 10.1002/ajmg.1320250626. Am J Med Genet Suppl. 1986. PMID: 3146293 Review.
The rare cases of fibuloulnar dimelia allow confirmation of the well known homology of mesomelic limb segments responsible for concordant ulnar and fibular (and radial and tibial) defect, if both upper and lower limbs are involved in a given condition. Because fibular a/hy …
The rare cases of fibuloulnar dimelia allow confirmation of the well known homology of mesomelic limb segments responsible for concordant …
Laurin-Sandrow Syndrome: A Case Report and Review of Literature.
Sathishkumar K, Anand S. Sathishkumar K, et al. J Hand Surg Asian Pac Vol. 2022 Aug;27(4):742-746. doi: 10.1142/S2424835522720389. Epub 2022 Aug 8. J Hand Surg Asian Pac Vol. 2022. PMID: 35965362 Review.
It is characterised by limb, facial and central nervous system anomalies with the most constant being fibular dimelia with fibular ray duplication, polydactyly with secondary deformities of fixed equinus, knee joint instability and flexion deformity. It is associated less frequen …
It is characterised by limb, facial and central nervous system anomalies with the most constant being fibular dimelia with fibular ray dupli …
Proximal focal femoral deficiency, contralateral hip dysplasia in association with contralateral ulnar hypoplasia and clefthand: a case report and review of literatures of PFFD and/or FFU.
Kalaycioglu A, Aynaci O. Kalaycioglu A, et al. Okajimas Folia Anat Jpn. 2001 Aug;78(2-3):83-9. doi: 10.2535/ofaj1936.78.2-3_83. Okajimas Folia Anat Jpn. 2001. PMID: 11732209 Review.
A 14 year old boy with proximal focal femoral deficiency (PFFD) on left side, contralateral hip dysplasia in association with ulnar hypoplasia and cleft hand was seen our clinic one year ago. ...
A 14 year old boy with proximal focal femoral deficiency (PFFD) on left side, contralateral hip dysplasia in association with ulnar h …
Humeroradial synostosis, ulnar aplasia and oligodactyly, with contralateral amelia, in a child with prenatal cocaine exposure.
Marles SL, Reed M, Evans JA. Marles SL, et al. Am J Med Genet A. 2003 Jan 1;116A(1):85-9. doi: 10.1002/ajmg.a.10731. Am J Med Genet A. 2003. PMID: 12476458 Review.
The family history was unremarkable, but he was exposed prenatally to cocaine at the time of limb development. Humeroradial synostosis with ulnar aplasia has been reported by several authors. The majority of cases are unilateral. ...
The family history was unremarkable, but he was exposed prenatally to cocaine at the time of limb development. Humeroradial synostosis with …