Split Hand/Foot Malformation with Long Bone Deficiency: A Report of Two Female Siblings
Spilt Hand/Foot Malformation with Long-bone Deficiency (SHFMLD) is a rare heterogeneous group of limb malformations characterised by absence/hypoplasia and/or median cleft of hands and/or feet associated with long bone abnormalities, most frequently tibia. This case report described two sisters wi...
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doaj-69214a8ac6b142d0afe05ad6b4f2515d2021-07-08T10:48:14ZengJCDR Research and Publications Private LimitedJournal of Clinical and Diagnostic Research2249-782X0973-709X2021-06-01156SD04SD0610.7860/JCDR/2021/48104.15060Split Hand/Foot Malformation with Long Bone Deficiency: A Report of Two Female SiblingsMohammed ALI Al-SHEHAB0Ahmed Saleh Hudna1Fahd Naji Thawaba2Farouk Abdulrahman Al-QADASI3Senior Specialist, Department of Paediatrics, University of Science and Technology Hospital, Sana’a, Yemen.Assistant Professor, Department of Paediatrics, University of Science and Technology, Sana’a, Yemen.Consultant, Department of Radiology, University of Science and Technology Hospital, Sana’a, Yemen.Master Degree in Epidemiology and Medical Statistics, Department of Statistics, International Organisation of Migration, Sana’a, Yemen.Spilt Hand/Foot Malformation with Long-bone Deficiency (SHFMLD) is a rare heterogeneous group of limb malformations characterised by absence/hypoplasia and/or median cleft of hands and/or feet associated with long bone abnormalities, most frequently tibia. This case report described two sisters with congenital limb defects born to healthy consanguineous parents. The six-year-old girl did not had both radii and the left fibula. There was a cleft in the left hand and the right foot. She had one digit in her right upper limb, but did not have the left foot. The four-year-old girl had short four limbs, bilateral tibial aplasia with single digit in all limbs. Both parents were normal, and no other similar cases was reported in the family. According to the authors' best knowledge, these two cases are the first published cases in Yemen with the SHFMLD, but they need a genetic study to determine their genetic profile.https://jcdr.net/articles/PDF/15060/48104_CE[Ra1]_F[IK]_PF1(AG_SK)_PN(KM).pdfconsanguinityectrodactylyyemen |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Mohammed ALI Al-SHEHAB Ahmed Saleh Hudna Fahd Naji Thawaba Farouk Abdulrahman Al-QADASI |
spellingShingle |
Mohammed ALI Al-SHEHAB Ahmed Saleh Hudna Fahd Naji Thawaba Farouk Abdulrahman Al-QADASI Split Hand/Foot Malformation with Long Bone Deficiency: A Report of Two Female Siblings Journal of Clinical and Diagnostic Research consanguinity ectrodactyly yemen |
author_facet |
Mohammed ALI Al-SHEHAB Ahmed Saleh Hudna Fahd Naji Thawaba Farouk Abdulrahman Al-QADASI |
author_sort |
Mohammed ALI Al-SHEHAB |
title |
Split Hand/Foot Malformation with Long Bone Deficiency: A Report of Two Female Siblings |
title_short |
Split Hand/Foot Malformation with Long Bone Deficiency: A Report of Two Female Siblings |
title_full |
Split Hand/Foot Malformation with Long Bone Deficiency: A Report of Two Female Siblings |
title_fullStr |
Split Hand/Foot Malformation with Long Bone Deficiency: A Report of Two Female Siblings |
title_full_unstemmed |
Split Hand/Foot Malformation with Long Bone Deficiency: A Report of Two Female Siblings |
title_sort |
split hand/foot malformation with long bone deficiency: a report of two female siblings |
publisher |
JCDR Research and Publications Private Limited |
series |
Journal of Clinical and Diagnostic Research |
issn |
2249-782X 0973-709X |
publishDate |
2021-06-01 |
description |
Spilt Hand/Foot Malformation with Long-bone Deficiency (SHFMLD) is a rare heterogeneous group of limb malformations
characterised by absence/hypoplasia and/or median cleft of hands and/or feet associated with long bone abnormalities, most
frequently tibia. This case report described two sisters with congenital limb defects born to healthy consanguineous parents. The
six-year-old girl did not had both radii and the left fibula. There was a cleft in the left hand and the right foot. She had one digit
in her right upper limb, but did not have the left foot. The four-year-old girl had short four limbs, bilateral tibial aplasia with single
digit in all limbs. Both parents were normal, and no other similar cases was reported in the family. According to the authors' best
knowledge, these two cases are the first published cases in Yemen with the SHFMLD, but they need a genetic study to determine
their genetic profile. |
topic |
consanguinity ectrodactyly yemen |
url |
https://jcdr.net/articles/PDF/15060/48104_CE[Ra1]_F[IK]_PF1(AG_SK)_PN(KM).pdf |
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