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Prof. mamoun Kremli DR: Gehan Mohamed.  Recognize some Limb Anomalies  Amelia, Meromelia, Hemimelia  Polydactyly  Syndactyly  Amniotic band syndrome.

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Presentation on theme: "Prof. mamoun Kremli DR: Gehan Mohamed.  Recognize some Limb Anomalies  Amelia, Meromelia, Hemimelia  Polydactyly  Syndactyly  Amniotic band syndrome."— Presentation transcript:

1 Prof. mamoun Kremli DR: Gehan Mohamed

2  Recognize some Limb Anomalies  Amelia, Meromelia, Hemimelia  Polydactyly  Syndactyly  Amniotic band syndrome  Discuss Etiology

3  Melia: from Greek: ”Limb”  Amelia: GK, A: Lack of..  Meromelia: Gk, meros: “part”: lack of part  Phocomelia:Gk, Phoco: “Seal”: like limb of Seal  Hemimelia: GK, Hemi: “Half”: lack of half of limb

4  Limbs arise from small limb buds  Upper limb bud appear after 26 days  Lower limb bud appear after 28 days.

5  Somatic lateral mesoderm →limb buds  (mesodermal core + ectodermal cap) →  elongated & fragmented → 3 portions

6 Wk 6  Terminal portions of limb buds form hand & foot plates  Digital rays in distal ends form fingers & toes (wk 8) (apoptosis of tissues in between)

7  Limb anomalies Are -prevented: Amelia -Interrupted: Meromelia. Phocomelia, Hemimelia  Very early in the developing embryo:  Between 24-36 days following fertilization

8  Absence of one or more limbs

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11 A. Environmental Factors 1. Teratogenic drugs ▪ e.g. Thalidiomide (was introduced as analgesic drug ) 2. Maternal Factors - Diabetes mellitus 3. Vascular accidents in uterus B. Genetics – 20% 1. Mutations in genes

12  Partial absence of a limb or limbs

13  Extremities resemble those of a seal.  Typically, hands and feet are present (may be normal or abnormal), but the intervening arms and legs are absent

14  Poly: many, dactyl: digit (finger/toe)  Presence of more than normal number of fingers or toes  Rudimentary finger or toe, or  Fully developed extra digit(s)

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18 18www.similima.com

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21  Most common congenital malformation of limbs  Incidence: 1 in 2000-3000

22  10-40 % are familial  Non hereditary non syndromic  Few reports association with maternal smoking

23  This type of mild syndactyly is found occasionally on the physical examination.  This is usually an isolated finding, and in this location, has no impact on function. 23www.similima.com

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29 Watson S Arch Dis Child 2000;83:10-17 Copyright © BMJ Publishing Group Ltd & Royal College of Paediatrics and Child Health. All rights reserved.  Hand with transverse deficiency at the metacarpal level.

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31  At a different plane  At 90 o to other fingers  Opposition motion  50% of hand function

32 Watson S Arch Dis Child 2000;83:10-17 Copyright © BMJ Publishing Group Ltd & Royal College of Paediatrics and Child Health. All rights reserved.  Pollicization of the index finger to make a thumb FatherChild after surgery

33 Watson S Arch Dis Child 2000;83:10-17 Copyright © BMJ Publishing Group Ltd & Royal College of Paediatrics and Child Health. All rights reserved.  Hand with thumb and aplastic fingers.

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35  The constriction of appendages by amniotic bands may result in:  Restrictions of the growth around the digits, arms and legs  Constriction rings around the digits, arms and legs  the bands will partially constrict the blood flow in the affected appendage causing a deep groove in the baby's skin  Swelling of the extremities distal to the point of constriction (congenital lymphedema)  Amputation of digits, arms and legs (congenital amputation)

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41 After surgery Before surgery

42  Partial fibular hemimelia  Short leg

43  Which is worse?  Why?

44  Which is worse?  Why?  Which bone is more important for knee and ankle joint surfaces?

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46  Many congenital anomalies  Nomenclature:  Amelia  Phocomelia, meromelia  Hemimelia  Polydatyly, Syndactyly  Amniotic band syndrome

47  Importance of thumb  50% of hand function  Tibial hemimelia Vs. Fibular hemimelia

48  Causes od anomalies:  Teratogenic Drugs  Uterine problems ▪ Blood supply (vascular accidents)  Maternal factors ▪ Disease: Diabetes ▪ Smoking, Alcohol  Hereditary


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